Therapeutic targets for Alzheimer&#39;s disease

ABSTRACT

The present invention relates to novel methods for the prevention, treatment and diagnosis of Alzheimer&#39;s disease. In addition, the invention relates to methods for assessing an individual&#39;s susceptibility or pre-disposition to Alzheimer&#39;s disease. The methods of the present invention involve the use of therapeutic targets and diagnostic and/or predictive markers within the mTOR signalling pathway. The methods also involve screening subjects for genetic polymorphisms associated with rapamycin-sensitive genes.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 14/413,659, filed Jan. 8, 2015, which is a § 371 of International Application No. PCT/GB2013/051843, filed Jul. 11, 2013, which claims priority from GB 1212334.5, filed Jul. 11, 2012. The entire disclosure of each of the aforesaid applications is incorporated by reference in the present application.

FIELD OF THE INVENTION

The present invention relates to novel strategies for the prevention, treatment and diagnosis of Alzheimer's disease. In addition, the invention relates to strategies for assessing an individual's susceptibility or pre-disposition to Alzheimer's disease. In particular, the present invention relates to methods involving the use of therapeutic targets and diagnostic and/or predictive markers within the mTOR signalling pathway.

BACKGROUND TO THE INVENTION

Alzheimer's disease is the most common form of dementia in older people. As a result of population aging worldwide, the prevalence of this disease is set to increase significantly in coming years. As such, there is an urgent need to develop better prognostic and diagnostic tools and new treatments for people identified as having this disease.

Alzheimer's disease is a chronic neurodegenerative disorder characterised by selective loss of cortical neurons within the hippocampus and the temporal and frontal lobes of the brain. The neurodegenerative process occurring in Alzheimer's disease is accompanied by progressive cognitive impairment leading ultimately to dementia in affected individuals.

There is currently no accepted “gold standard” diagnostic test for Alzheimer's disease in the live patient. This reflects the difficulties associated with identifying patients who would go on to be classified as having this disease at post mortem examination. Clinical diagnosis of Alzheimer's disease is typically based on evaluation of clinical criteria, such as the NINCDS/ADRDA criteria (McKhann, G. et al., (1984) Neurology 34: 939-944).

The problem with the diagnostic methods used to date lies in the fact that patients are typically diagnosed once clinical dementia has started to develop. It follows therefore, that existing treatment strategies are limited to agents used primarily to manage the symptoms of disease. For example, cholinesterase inhibitors are administered to patients so as to block the degradation of the neurotransmitter acetylcholine and thereby enhance neurotransmission in the brain. Use of such agents can help to preserve cognitive function, but does not improve the underlying pathology and is therefore not a curative approach.

Although the etiology of Alzheimer's disease is poorly understood, the neuropathology associated with the development of this disease has been relatively well characterised. The classical hallmarks of this disease consist of amyloid-β plaques, which accumulate in the brain, and neurofibrillary tangles (NFT) consisting of hyperphosphorylated tau protein present in affected neurons. Additional changes occurring at the cellular level, which are now thought to precede the deposition of plaques and NFTs, include damage to cells caused by oxidative stress, mitochondrial malfunction and aberrant re-entry of neurons into the cell division cycle.

In addition to difficulties associated with diagnosing Alzheimer's disease, there are also problems associated with identifying individuals in the population who are at increased and/or decreased risk of developing Alzheimer's disease during their lifetime, as compared with the average level of risk associated with the general population. The only known genetic risk factor for late onset sporadic form of Alzheimer's disease is the polymorphism on the ApoE gene. Other discovered polymorphisms appear to be restricted to relatively small patient subgroups. Thus risk prediction or assessment of susceptibility, before the development of clinical Alzheimer's disease, is difficult as well.

There is now good evidence to suggest that the neuropathology underlying Alzheimer's disease begins years, maybe even a decade, prior to the diagnosis of clinical dementia (Forlenza et al., (2010) BMC Medicine 8:89). Based on these observations, the continuum of Alzheimer's disease progression has been classified into three phases:

(i) asymptomatic Alzheimer's disease (preclinical stage);

(ii) mild cognitive impairment (MCI) due to Alzheimer's disease (pre-dementia stage); and

(iii) clinically-defined Alzheimer's disease (dementia).

In light of the above, there now exist several opportunities for improved management of Alzheimer's disease. In particular, it may be possible to identify individuals at increased risk of developing Alzheimer's disease, and/or diagnose individuals at a much earlier stage of disease, for example, individuals with asymptomatic disease or those patients with MCI that will go on to develop clinically-defined Alzheimer's disease. If susceptible individuals can be identified and/or diagnosed at an earlier stage of disease, it will be possible to develop, test and use new preventative and/or curative treatments intended to stabilize and/or reverse the neurodegenerative process and thereby prevent cognitive decline.

Researchers are already using the improved knowledge of Alzheimer's disease pathogenesis to develop more effective methods of diagnosis and treatment. In this regard, diagnostic biomarkers have been identified that can be measured in humoral fluids, mainly cerebrospinal fluids, and biomarkers that may be detected using advanced neuroimaging methods (Gustaw-Rothenberg et al., (2010) Biomark. Med. 4(1):15-26).

Furthermore, new “disease-modifying” treatments are being developed that tackle the deposition of β-amyloid plaques and NFTs (Bonda et al., (2010) Curr. Opin. Drug Discov Devel. 13(2): 235-246)

There remains however, an ongoing need to improve methods for the diagnosis and treatment of Alzheimer's disease, particularly early-stages of disease. The present invention seeks to address these issues.

SUMMARY OF INVENTION

The present invention is directed towards new methods of preventing, treating and diagnosing Alzheimer's disease based on the use of novel gene targets linked to this disease. The invention also relates to screening methods for identifying individuals that are pre-disposed to Alzheimer's disease, based on the use of novel gene targets.

The gene targets presented herein are classified as “rapamycin-sensitive” genes for the reason that their cellular expression is affected by the compound rapamycin. The group of rapamycin-sensitive genes to which the present invention relates were found to be deregulated in the brains of patients diagnosed with Alzheimer's disease, as compared with control samples, using microarray expression analysis. Rapamycin is known to inhibit the serine/threonine kinase mTOR and thereby reduce signalling downstream of this protein therefore the present invention is directed in particular, to the use of novel therapeutic and diagnostic targets within the mTOR signalling pathway in the context of methods for the prevention, treatment and diagnosis of Alzheimer's disease.

In a first aspect, the present invention provides a method for the prevention and/or treatment of Alzheimer's disease in a subject, comprising administering to the subject a pharmacological agent which modulates one or more targets within the mTOR signalling pathway of a cell, wherein the target is selected from:—

-   -   (i) the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (ii) the transcriptional products of the rapamycin-sensitive         genes shown in Tables 2, 3, 4 and 5, or fragments thereof; and     -   (iii) the proteins encoded by the rapamycin-sensitive genes         shown in Tables 2, 3, 4 and 5, or fragments thereof.

In a second aspect, the invention provides a method of screening for pharmacological agents useful in the prevention and/or treatment of Alzheimer's disease in a subject, wherein said method comprises:—

-   -   (i) contacting a cell with a test pharmacological agent;         -   (ii) measuring either the expression level of one or more of             the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5,             or the level or activity of one or more of the proteins             encoded by the rapamycin-sensitive genes shown in Tables 2,             3, 4 and 5;         -   (iii) measuring either the expression level of one or more             of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and             5, or the level or activity of one or more of the proteins             encoded by the rapamycin-sensitive genes shown in Tables 2,             3, 4 and 5 in a control cell not exposed to the test             pharmacological agent;         -   (iv) comparing the results determined in steps (ii) and             (iii)     -   wherein a difference in the expression level of one or more of         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or         the level or activity of one or more of the proteins encoded by         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5,         indicates that the test pharmacological agent is suitable for         use in the prevention and/or treatment of Alzheimer's disease.

In a third aspect, the invention provides a method to assist with diagnosis of Alzheimer's disease in a live human subject, which method comprises the steps of:—

-   -   (i) measuring either the expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or         the activity of one or more of the proteins encoded by the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (ii) comparing the expression level and/or activity measured         in (i) with reference/control values,     -   wherein a difference in expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or         the level or activity of one or more of the proteins encoded by         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 is         indicative of Alzheimer's disease.

In a fourth aspect, the invention provides a method of assessing the risk of Alzheimer's disease progression in a human subject, which method comprises the steps of:—

-   -   (i) measuring either the expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or         the activity of one or more of the proteins encoded by the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (ii) comparing the expression level and/or activity measured         in (i) with reference/control values,         wherein a difference in expression level and/or activity of the         one or more rapamycin sensitive genes shown in Tables 2, 3, 4         and 5 is indicative of Alzheimer's disease progression.

In a fifth aspect, the invention provides a method for screening a human subject for pre-disposition to Alzheimer's disease, which method comprises the steps of:—

-   -   (i) measuring either the expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or         the activity of one or more of the proteins encoded by the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (ii) comparing the expression level and/or activity measured         in (i) with reference/control values,         wherein a difference in expression level and/or activity of the         one or more rapamycin sensitive genes shown in Tables 2, 3, 4         and 5 is taken to mean the subject is pre-disposed to         Alzheimer's disease.

In all aspects of the invention described above, in preferred embodiments, the one or more targets within the mTOR signalling pathway is/are selected from the group of rapamycin-sensitive genes consisting of calcium channel, voltage-dependent, L type, alpha 1D subunit (CACNA1D), gamma-aminobutyric acid B receptor, 2 (GABBR2), homeobox D10 (HOXD10), Kruppel-like factor 2 (KLF2), rhodopsin (RHO) and GLI zinc finger family 2 (GLI2).

The present invention is also directed to methods for identifying human subjects that are pre-disposed to Alzheimer's disease, and methods to assist with diagnosis of Alzheimer's disease in live human subjects based on the use of polymorphisms, particularly single nucleotide polymorphisms (SNPs), in the rapamycin-sensitive genes described herein. Methods are also described based on the use of polymorphisms within genes which affect the expression of rapamycin-sensitive genes.

Therefore, in a sixth aspect, the invention provides a method of screening a human subject for pre-disposition to Alzheimer's disease, which method comprises genotyping the subject for one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

In a seventh aspect, the invention provides a method of screening a human subject for pre-disposition to Alzheimer's disease, which method comprises genotyping the subject for one or more polymorphisms in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

In an eighth aspect, the invention provides a method to assist with diagnosis of Alzheimer's disease in a live human subject, which method comprises genotyping the subject for one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, or a polymorphism in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is indicative of Alzheimer's disease.

In a ninth aspect, the invention provides an array or kit for detecting genetic polymorphisms in a sample taken from a subject wherein the array or kit comprises reagents for the detection of one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, or one or more polymorphisms in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1.

The present invention is also concerned with polymorphisms that may be used to monitor the mTOR signalling pathway in a cell. These polymorphisms are associated with the differential sensitivity of cells to the G1/S inhibitor rapamycin.

Therefore, in a further aspect, the invention provides a method by which to monitor mTOR signalling in a human cell, which method comprises detecting one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, or one or more polymorphisms in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with a differential response to rapamycin is indicative of the status of mTOR signalling in the cell.

In all aspects of the invention relating to polymorphisms described above, in preferred embodiments, the one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms for the purposes of genotyping or detection are in one or more of the rapamycin-sensitive genes selected from LILRB2, FAM5C, CRP, CLU, FCGR2A, CD1E, FAM5C, LPL, SYK and CUX1 and/or in one or more of the genes which affect the expression of one or more rapamycin-sensitive genes, selected from POU2F1, ADRA1A, PRDM1 and LOXL2.

In further preferred embodiments, the one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms is/are selected from the group consisting of:

-   -   (i) the single polynucleotide polymorphisms: rs798893, rs725106,         rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925,         rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and         rs569214; and     -   (ii) any polymorphism in linkage disequilibrium with the single         nucleotide polymorphisms of (i).

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 Cell cycle dependent expression of phosphor-tau (p-tau) in SH-SY5Y neuroblastoma cells. White bars=G1; Black bars=G2.

FIG. 2 Effect of rapamycin on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=control cells treated with culture medium; Darker shading=cells treated with 100 ng/ml rapamycin.

FIG. 3 Effect of rapamycin on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=control cells treated with culture medium; Darker shading=cells treated with 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 4 Effect of siRNA-mediated down-regulation of CACNA1D on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and CACNA1D siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 5 Effect of siRNA-mediated down-regulation of CACNA1D on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and CACNA1D siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 6 Effect of siRNA-mediated down-regulation of GABBR2 on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and GABBR2 siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 7 Effect of siRNA-mediated down-regulation of GABBR2 on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and GABBR2 siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 8 Effect of siRNA-mediated down-regulation of HOXD10 on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and HOXD10 siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 9 Effect of siRNA-mediated down-regulation of HOXD10 on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and HOXD10 siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 10 Effect of siRNA-mediated down-regulation of KLF2 on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and KLF2 siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 11 Effect of siRNA-mediated down-regulation of KLF2 on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and KLF2 siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 12 Effect of siRNA-mediated down-regulation of RHO on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and RHO siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 13 Effect of siRNA-mediated down-regulation of RHO on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and RHO siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 14 Effect of siRNA-mediated down-regulation of GL12 on cell cycle kinetics in SH-SY5Y neuroblastoma cells. Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and GL12 siRNA alone; Darker shading=cells treated with additional 100 ng/ml rapamycin.

FIG. 15 Effect of siRNA-mediated down-regulation of GL12 on p-tau expression in SH-SY5Y neuroblastoma cells. Grey bars=all single cells; Vertically-shaded bars=G1 population; Horizontally-shaded bars=G2 population; Lighter shading=cells treated with Culture medium, siRNA Control and GL12 siRNA alone; Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%).

FIG. 16 T₂ weighted MRI images of (A) rapamycin-treated animals, (B) ketamine-treated animals and (C) control animals.

FIG. 17 The effect of mTOR modulation on phosphatidylcholine species in the brain.

FIG. 18 The effect of mTOR modulation on choline (A) and creatine (B) levels in the brain.

DETAILED DESCRIPTION

The present invention is directed to methods for preventing, treating and/or diagnosing Alzheimer's disease in live human subjects involving use of gene targets within the “mTOR signalling pathway”.

The kinase, “mTOR”, functions within the context of two cytoplasmic protein complexes known as mTORC1 and mTORC2. It is however, only the mTORC1 complex that is sensitive to the inhibitor rapamycin. Thus, the targets of interest in the present invention may also be classified as targets within the mTORC1 signalling pathway.

The cytoplasmic kinase mTOR is stimulated or activated by a wide variety of upstream signals. These include signals generated or triggered as a result of nutrient sensing, hypoxia, and/or the activity of growth factors and their cognate receptors. Activation of mTOR upregulates its kinase activity and thereby increases mTOR-mediated phosphorylation of downstream protein targets within the cell. In most cases, the direct downstream protein targets of mTOR interact with a variety of further molecular targets, and in doing so, stimulate a wide variety of cellular responses, such as increased protein synthesis and the promotion of cell growth and proliferation. The chain of molecular events triggered downstream of mTOR-mediated phosphorylation of its direct protein targets is defined herein as the “mTOR signalling pathway”, and the target genes/proteins of the present invention fall within this pathway.

In the methods of the present invention, the particular targets of interest within the mTOR signalling pathway are selected from the genes shown in Tables 2, 3, 4 and 5. The term “target” is intended to encompass the genes of Tables 2, 3, 4 and 5, the transcriptional products of such genes and the proteins encoded by such genes.

The particular genes shown in Table 1 are “rapamycin-sensitive” for the reason that their cellular expression is affected (increased or decreased) by the compound rapamycin. Since rapamycin is known to inhibit the serine/threonine kinase mTOR in (human) cells, and thereby reduce signalling downstream of this protein, the genes shown in Tables 2, 3, 4 and 5 are grouped herein as targets within the mTOR signalling pathway. Tables 2 and 4 show the rapamycin-sensitive genes that have an altered expression in the brain of Alzheimer's patients with mild disease and Tables 3 and 5 show the rapamycin-sensitive genes that have an altered expression in the brain of Alzheimer's patients with advanced disease.

Therapeutic Methods

In a first aspect, the present invention provides methods for the prevention and/or treatment of live human subjects diagnosed with Alzheimer's disease involving administration of pharmacological agents which modulate or are capable of modulating one or more, two or more, three or more, four or more etc. targets within the mTOR signalling pathway.

In certain embodiments, the therapeutic target is selected from the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 and the pharmacological agent will typically modulate the target via effects at the level of gene expression. In preferred embodiments, the one or more targets within the mTOR signalling pathway is/are selected from the group of rapamycin-sensitive genes consisting of calcium channel, voltage-dependent, L type, alpha 1D subunit (CACNA1D), gamma-aminobutyric acid B receptor, 2 (GABBR2), homeobox D10 (HOXD10), Kruppel-like factor 2 (KLF2), rhodopsin (RHO) and GLI zinc finger family 2 (GL12).

In certain embodiments, the pharmacological agent may act by up-regulating/increasing or down-regulating/decreasing expression of the target gene. Gene expression may be detected at the level of the transcriptional product or at the level of the protein produced, using standard techniques described herein below. Up-regulation or down-regulation of gene expression is measured relative to the situation in the absence of pharmacological agent, or in the presence of an appropriate, inactive control.

In certain embodiments of the invention, the term “target” may be used to refer to the transcriptional products of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or fragments thereof. The term “transcriptional product” is intended to encompass the pre-mRNA species generated following transcription of the gene, any of the splice intermediates generated during pre-mRNA processing and the mature fully-spliced mRNA species. Inhibition of such transcriptional products may involve down-regulating the level of such products, for example, by promoting nucleic acid degradation. This may be mediated for example, by interfering RNA species, such as siRNAs.

In certain other embodiments of the invention, the “target” may refer to the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or fragments thereof. The pharmacological agent may therefore bring about an increase or decrease in the level of protein within a cell or an increase or decrease in the biological activity of the protein.

As noted above, the target of the invention may include a fragment of the transcriptional product of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 or a fragment of a protein encoded by one or more of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5. The term “fragment” should be taken to mean a form of the transcriptional product or protein, which is reduced in length by one or more, two or more, three or more, four or more etc. nucleotides or amino acids, respectively, as compared with the full-length transcriptional product or protein. In relation to post-transcriptional products, the term “fragment” may also be applied to alternatively-spliced forms of mRNA produced from the originating pre-mRNA transcript.

In the context of the present invention, the term “modulates” is used very broadly to mean an agent capable of changing or altering the expression of a gene, the production and/or level of a transcriptional product of a gene and/or the production, level and/or activity of a protein encoded by a gene. The term “modulates” may be used to describe an increase or a decrease in any of the parameters described above. Any increase or decrease is measured relative to the situation present in the absence of the pharmacological agent or in the presence of a suitable inactive control.

In one embodiment, the pharmacological agent is an activator or agonist capable of increasing or up-regulating the expression of a gene, the production and/or level of a transcriptional product of a gene and/or the production, level and/or activity of a protein encoded by a gene. In an alternative embodiment, the pharmacological agent is an inhibitor or antagonist capable of decreasing or down-regulating the expression of a gene, the production and/or level of a transcriptional product of a gene and/or the production, level and/or activity of a protein encoded by a gene.

Classes of pharmacological agents suitable for use in accordance with the methods described herein would be available to those skilled in the art. Such agents include but are not limited to small molecules, organic or inorganic molecules, biological molecules including antibodies and antigen binding fragments thereof, natural or synthetic polypeptides or peptides, nucleic acid therapeutic agents including antisense RNA species and double-stranded RNA species for use as RNA interfering agents, for example siRNA molecules.

In the context of the present invention, the term antibody covers native immunoglobulins from any species, chimeric antibodies, humanised antibodies, F(ab′)2 fragments, Fab fragments, Fv fragments, sFv fragments and highly related molecules such as those based upon antibody domains which retain specific binding affinity (for example, single domain antibodies).

Pharmacological agents may be formulated as compositions for delivery wherein the agent in a suitable dosage form is combined with a pharmaceutically acceptable carrier such as a diluent, filler, salt, buffer, stabilizer, solubilizer etc. The dosage form may contain other pharmaceutically acceptable excipients for modifying conditions such as pH, osmolarity, taste, viscosity, sterility, lipophilicity, solubility etc.

Suitable dosage forms include solid dosage forms, for example, tablets, capsules, powders, dispersible granules, cachets and suppositories, including sustained release and delayed release formulations. Powders and tablets will generally comprise from about 5% to about 70% active ingredient. Suitable solid carriers and excipients are generally known in the art and include, e.g. magnesium carbonate, magnesium stearate, talc, sugar, lactose, etc. Tablets, powders, cachets and capsules are all suitable dosage forms for oral administration.

Liquid dosage forms include solutions, suspensions and emulsions. Liquid form preparations may be administered by intravenous, intracerebral, intraperitoneal, parenteral or intramuscular injection or infusion. Sterile injectable formulations may comprise a sterile solution or suspension of the active agent in a non-toxic, pharmaceutically acceptable diluent or solvent. Suitable diluents and solvents include sterile water, Ringer's solution and isotonic sodium chloride solution, etc. Liquid dosage forms also include solutions or sprays for intranasal administration.

Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be combined with a pharmaceutically acceptable carrier, such as an inert compressed gas.

Also encompassed are dosage forms for transdermal administration, including creams, lotions, aerosols and/or emulsions. These dosage forms may be included in transdermal patches of the matrix or reservoir type, which are generally known in the art.

Pharmaceutical preparations may be conveniently prepared in unit dosage form, according to standard procedures of pharmaceutical formulation. The quantity of active compound per unit dose may be varied according to the nature of the active compound and the intended dosage regime. Generally this will be within the range 0.1 mg to 1000 mg.

Wherein the pharmacological agent consists of a nucleic acid therapeutic agent, for example, an antisense RNA species or a double-stranded RNA species for use as an RNA interfering agent, the active agent may be administered to a patient in need thereof via gene therapy approaches.

The rapamycin-sensitive target genes shown in Tables 2, 3, 4 and 5 encode a range of proteins including enzymes, receptors and transporters. Preferred known pharmacological agents for use in conjunction with the present methods include the following; however, this is not to be construed as limiting the invention to these specific embodiments.

Wherein the target gene is CACNA1D, pharmacological agents for use may include MEM-1003, clevidipine butyrate, aliskiren/amlodipine/hydrochlorothiazide, mibefradil, bepridil, nisoldipine, isradipine, amlodipine and/or nicardipine.

Wherein the target gene is HDAC5, pharmacological agents for use may include tributyrin, belinostat, pyroxamide, vorinostat and/or romidepsin.

Wherein the target gene is IL6, pharmacological agents for use may include tocilizumab.

Wherein the target gene is NR3C1, pharmacological agents for use may include rimexolone, medrysone, clocortolone pivalate, diflorasone diacetate, fluorometholone, dexamethasone phosphate, cortisone acetate, halcinonide, flurandrenolide, desoximetasone, desonide, prednisolone, clobetasol propionate, fluocinolone acetonide, prednisone, hydrocortisone, triamcinolone, dexamethasone 21-acetate, 11 beta hydrocortisone acetate, betamethasone, dexamethasone, budesonide, fluticasone, beclomethasone dipropionate, acetic acid/hydrocortisone, betamethasone acetate/betamethasone phosphate, betamethasone acetate, triamcinolone acetonide, ciprofloxacin/hydrocortisone, dexamethasone/neomycin/polymyxin B, ciprofloxacin/dexamethasone, ORG 34517, ciclesonide, betamethasone dipropionate/calcipotriene, fluticasone furoate, budesonide/formoterol, difluprednate, formoterol/mometasone furoate, clotrimazole/betamethasone dipropionate, fluticasone/salmeterol, dexamethasone/tobramycin, clotrimazole/betamethasone, miconazole, prednisolone acetate, clioquinol/hydrocortisone, methylprednisolone acetate, mometasone furoate, amcinonide, methylprednisolone succinate, betamethasone phosphate, fluocinonide, prednicarbate, hydrocortisone cypionate, hydrocortisone succinate, prednisolone phosphate, betamethasone valerate, betamethasone benzoate, fludrocortisone acetate, prednisolone tebutate, betamethasone dipropionate, hydrocortisone buteprate, alclometasone dipropionate, hydrocortisone butyrate, fluorometholone acetate, hydrocortisone valerate, nystatin/triamcinolone acetonide, loteprednol etabonate, hydrocortisone phosphate, methylprednisolone, halobetasol propionate, flunisolide and/or mifepristone.

Wherein the target gene is NTSR1, pharmacological agents for use may include contulakin-G.

Wherein the target gene is PRKCH, pharmacological agents for use may include ingenol 3-angelate.

Wherein the target gene is SCN8A, pharmacological agents for use may include riluzole.

Wherein the target gene is SERPINE1, pharmacological agents for use may include drotrecogin alfa.

Wherein the target gene is TRPV1, pharmacological agents for use may include SB-705498, resiniferatoxin and/or capsaicin.

Wherein the target gene is VEGFA, pharmacological agents for use may include bevacizumab, ranibizumab, aflibercept and/or pegaptanib.

Wherein the target gene is GLP1R, pharmacological agents for use may include liraglutide, T-0632, GLP-1 (7-36) amide and/or exenatide.

The term “Alzheimer's disease” is used herein broadly to mean disease diagnosed on the basis of clinical criteria and/or disease identified on the basis of pathophysiological changes associated with AD.

At present, the diagnosis of Alzheimer's disease in live human subjects is based on the evaluation of clinical criteria, such as the NINCDS/ADRDA criteria (McKhann, G. et al., (1984) Neurology 34: 939-944). However, such diagnostic criteria applied in the clinic are based on the measurement of cognitive parameters, and are thus reliant on the onset of cognitive symptoms in patients with this disease.

It is however, clear from extensive research carried out that the pathophysiological or changes defining AD are detectable in individuals years before these patients show any signs of cognitive impairment. Alzheimer's disease has accordingly, been classified into three phases:

-   -   (i) asymptomatic Alzheimer's disease (preclinical stage);     -   (ii) mild cognitive impairment (MCI) due to Alzheimer's disease         (pre-dementia stage); and     -   (iii) clinically-defined Alzheimer's disease (dementia).

In the context of the present invention, the phrase “prevention and/or treatment of Alzheimer's disease” is intended to encompass prevention and/or treatment strategies used for an individual having disease at any one of the three phases defined above.

It is not at present possible to reliably diagnose individuals with asymptomatic AD or early-stage disease; however, as methods of diagnosis improve, it may prove possible to identify individuals with neuropathological changes defining the early stages of AD. The methods described herein may therefore be used to prevent and/or delay the onset of cognitive symptoms in a subject asymptomatic for Alzheimer's disease. This may be achieved by a reversal, stabilisation and/or delay of the neurological changes underlying AD pathology.

The methods provided herein may also be used to prevent and/or delay the onset of AD-associated dementia in individuals who are already symptomatic to varying degrees. For example, the methods of the invention may be applied to individuals classified according to standard criteria, for example the Mayo Clinic diagnostic criteria (Winblad et al., (2004) J. Intern. Med 256: 240-246), as having mild cognitive impairment (MCI). In a further embodiment, the method of the invention may be used to prevent and/or delay the worsening of symptoms in individuals already diagnosed with clinical dementia. The methods of the present invention may therefore be used to treat Alzheimer's disease in a subject exhibiting mild cognitive impairment or in a subject exhibiting clinical dementia.

The human subject to be treated according to the methods provided herein may be any human subject diagnosed as having Alzheimer's disease. This includes individuals with early-onset familial Alzheimer's disease and individuals with late-onset sporadic forms of this disease.

Screening Methods

In a second aspect, the present invention also provides methods of screening for pharmacological agents useful in the prevention and/or treatment of Alzheimer's disease in a subject, wherein said method comprises the steps of:—

-   -   (i) contacting a cell with a test pharmacological agent;     -   (ii) measuring either the expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or the         level or activity of one or more of the proteins encoded by the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (iii) measuring either the expression level of one or more of         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or         the level or activity of one or more of the proteins encoded by         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 in a         control cell not exposed to the test pharmacological agent;     -   (iv) comparing the results determined in steps (ii) and (iii)     -   wherein a difference in the expression level of one or more of         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, or         the level or activity of one or more of the proteins encoded by         the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5,         indicates that the test pharmacological agent is suitable for         use in the prevention and/or treatment of Alzheimer's disease.

In preferred embodiments, the one or more targets within the mTOR signalling pathway is/are selected from the group of rapamycin-sensitive genes consisting of calcium channel, voltage-dependent, L type, alpha 1D subunit (CACNA1D), gamma-aminobutyric acid B receptor, 2 (GABBR2), homeobox D10 (HOXD10), Kruppel-like factor 2 (KLF2), rhodopsin (RHO) and GLI zinc finger family 2 (GL12).

The pharmacological agents for testing in the screening methods provided herein may be selected from any class of agent as described in the context of the therapeutic methods of the present invention. The methods may involve screening one or more pharmacological agents simultaneously, for example in a multiplex format. Agents for use in the screening methods may be provided in any suitable format, including compound libraries.

The “difference” in gene expression and/or protein activity to be detected using the screening method described herein may be established according to the sensitivity requirements of those using the method to identify pharmacological agents suitable for the prevention and/or treatment of AD.

In certain embodiments, the difference may be measured as a decrease in the expression of one or more of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 as compared with control cells not exposed to the pharmacological agent, wherein said decrease indicates that the test pharmacological agent is suitable for use in the prevention and/or treatment of Alzheimer's disease.

Any difference or decrease in gene expression may be measured by assessing the level of transcriptional product or mRNA produced from any of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5. Alternatively or in addition, any difference or decrease may be measured by assessing the levels of protein produced from any of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5.

Suitable methods for the detection/quantitation of transcriptional products which may be used in accordance with the present methods are well known in the art, and include, but are not limited to hybridisation techniques, such as Northern blotting or microarray technologies, and amplification-based techniques such as RT-PCR or nucleic-acid sequence-based amplification (NASBA).

Suitable techniques for assessing protein levels are known in the art and include, but are not limited to, flow cytometry, immunoblot analysis, ELISA, Elispot and Fluorospot assays. In certain embodiments, these assays may be used in conjunction with commercially-available antibodies that bind to the protein of interest, in order to determine protein levels. Standard assays are also available for measuring the activity of certain proteins, for example standard enzyme activity assays, such as kinase assays.

Diagnostic Methods

In a further aspect, the current invention provides a method to assist with diagnosis of Alzheimer's disease in a live human subject.

In the context of the present invention, the term “diagnosis of Alzheimer's disease” is used very broadly and should be taken to mean diagnosis of an individual having disease at any one of the three phases of the disease defined above i.e. the preclinical stage, the pre-dementia stage or the dementia stage. In one embodiment, the method of the invention is used to diagnose or assist with diagnosis of Alzheimer's disease in its preclinical stage in an individual with no symptoms of disease, for example no signs of cognitive impairment. In other embodiments, the same basic methodology may be used to screen subjects who are “symptomatic” to varying degrees. For example, the method of the invention may be applied to individuals classified according to standard criteria, for example the Mayo Clinic diagnostic criteria (Winblad et al., (2004) J. Intern. Med 256: 240-246), as having mild cognitive impairment (MCI). Not all patients classified as having MCI will have the type of underlying neurodegeneration associated with Alzheimer's disease. Thus, the present method may be used to distinguish or assist with distinguishing between individuals with MCI that have underlying Alzheimer's disease and therefore are likely to go on to develop Alzheimer's disease-associated dementia, and those that have MCI attributable to a different cause or condition. In a further embodiment of the invention, the method may be used to diagnose or assist with diagnosis of Alzheimer's disease in a human subject exhibiting one or more symptoms consistent with Alzheimer's disease.

The diagnostic methods of the present invention may also be used in conjunction with existing diagnostic criteria, for example the NINCDS/ADRDA criteria, in order to verify or substantiate an Alzheimer's disease diagnosis in a human subject who already meets the existing criteria for a positive diagnosis. In this embodiment, the present methods may provide an adjunct to alternative diagnostic tests, wherein the present methods are independent of neuropsychological symptoms. This may allow for a more reliable diagnosis of clinical Alzheimer's disease, particularly since not all patients presenting with dementia symptoms will have Alzheimer's disease as the underlying cause.

The present methods are used in particular, to assist with diagnosis of Alzheimer's disease in a live human subject. A definitive diagnosis of Alzheimer's disease is generally considered by those in the field to be impossible in a live subject, and can only be made post-mortem following pathological examination of brain tissue from the patient. Thus, although present methods may seek to “diagnose” Alzheimer's disease in live subjects, such a diagnosis is typically based on an assessment of the likelihood that any given individual has the disease. In this regard, individuals may be classified as “possible Alzheimer's disease” or “probable Alzheimer's disease” based on the results of current diagnostic tests.

The present methods may therefore be used to “assist with diagnosis” meaning that they are used to assess the likelihood that an individual has Alzheimer's disease at any one of the three phases of the disease described above. In preferred embodiments, the present method may be used to assist with diagnosis of early-stage Alzheimer's disease in asymptomatic patients or patients exhibiting mild cognitive impairment.

The methods of the invention may also be used in combination or together with other methods or tests used for Alzheimer's disease diagnosis, for example in order to improve the specificity and/or sensitivity of these methods or tests. In specific embodiments, the present methods may be carried out in combination with a test designed to monitor one or more biomarkers of Alzheimer's disease in a particular individual, and the combined result may be used to assess the likelihood that the individual has Alzheimer's disease. In alternative embodiments, the present method may be used to independently substantiate the results of other diagnostic tests.

The present method is intended to provide a means to diagnose and/or assist with diagnosis of Alzheimer's disease in multiple settings. In one embodiment, the present method may be used to diagnose individuals with Alzheimer's disease so as to identify patients suitable for the assessment of new Alzheimer's disease treatments, for example the identification of suitable subjects for clinical trials. New treatments or therapies designed to be preventive and/or curative may only have the best chance of success in patients with asymptomatic or early-stage disease. The present method may therefore be used to diagnose or assist with diagnosis of preclinical Alzheimer's disease in asymptomatic individuals or to diagnose or assist with diagnosis of individuals with MCI that have underlying Alzheimer's disease pathology, for the purposes of assessing new treatments specifically in these patients. As improved treatments for Alzheimer's disease become available, the present methods may also be used to diagnose or assist with diagnosis of individuals so as to identify patients who will benefit from treatments that may have the ability to prevent cognitive decline.

The present invention also provides methods of assessing the risk of Alzheimer's disease progression in a human subject. In this context, “Alzheimer's disease progression” should be taken to mean the progressive neurodegeneration associated with this disease and/or the progressive decline in cognitive function that accompanies the underlying neuropathology. Such methods may be applied to individuals suspected of having any one of the three phases of Alzheimer's disease defined above, or individuals considered at risk of developing this disease.

In preferred embodiments of the invention, the methods provide means by which to assess or predict cognitive decline in human subjects by identifying individuals with early-stage Alzheimer's disease who will go on to develop Alzheimer's disease-associated dementia. In certain embodiments, the individual or human subject for testing will be asymptomatic for Alzheimer's disease. In alternative embodiments, the individual or human subject for testing will exhibit mild cognitive impairment or will exhibit one or more symptoms consistent with Alzheimer's disease.

In the diagnostic methods and the methods of assessing the risk of disease progression described above, the method comprises as a first step measuring either the expression level of one or more of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 and/or the activity of one or more of the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5. Gene expression may be analysed by assessing levels of mRNA produced following gene transcription or by assessing levels of the protein produced following translation of the mRNA. The detection of mRNA and protein levels may be carried out by methods known to those skilled in the art. Protein activity may also be analysed using suitable assays known to those skilled in the art.

In certain embodiments of the invention, protein activity may be measured directly. For example, the activity of a kinase enzyme may be measured using an assay that detects phosphorylation of the enzyme's direct substrate. Protein activity may also be measured indirectly by measuring alterations and/or changes in the level and/or activity of metabolites linked to the activity of the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5.

As a second step, the methods require a comparison between the gene expression levels and/or protein activity measured in the first step and the gene expression levels and/or protein activity defined as reference or control values. Such reference or control values may be determined from measurements made using age-matched healthy subjects, preferably wherein such subjects exhibit no signs of cognitive impairment. If the method is carried out with the intention of assessing the risk of Alzheimer's disease progression, the reference or control values may consist of values determined from measurements made using the same human subject at an earlier point in time, for example 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or 11 months earlier, or 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 etc years earlier. A comparison between measurements determined for the same human subject at different points in time may assist in determining whether there has been a change in the level of expression of a gene and/or activity of a protein over time that is indicative of Alzheimer's disease progression.

The genes and/or proteins for use in conjunction with the diagnostic methods of the present invention are selected from the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5. In preferred embodiments, the one or more targets within the mTOR signalling pathway is/are selected from the group of rapamycin-sensitive genes consisting of calcium channel, voltage-dependent, L type, alpha 1D subunit (CACNA1D), gamma-aminobutyric acid B receptor, 2 (GABBR2), homeobox D10 (HOXD10), Kruppel-like factor 2 (KLF2), rhodopsin (RHO) and GLI zinc finger family 2 (GL12).

The measurement of gene expression and/or protein activity may be made using any suitable sample taken from the subject. In a preferred embodiment, the sample is derived from the cerebrospinal fluid of a patient. In certain embodiments, the level or gene expression and/or protein activity may be determined using imaging techniques, preferably non-invasive imaging of the subject's brain or regions thereof. In certain embodiments, imaging techniques may be used to detect alterations and/or temporal changes in brain metabolites, such as choline or creatine, that are indicative of a change in protein activity. Imaging techniques that may be particularly useful in conjunction with the present methods include but are not limited to PET, SPECT, MR spectroscopy and functional MRI.

Methods of Assessing Pre-Disposition to Alzheimer's Disease

In a further aspect, the current invention also provides methods for screening a human subject for pre-disposition to Alzheimer's disease, wherein said method comprises the steps of:—

-   -   (i) measuring either the expression level of one or more of the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or         the activity of one or more of the proteins encoded by the         rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5;     -   (ii) comparing the expression level and/or activity measured         in (i) with reference/control values,     -   wherein a difference in expression level and/or activity of the         one or more rapamycin sensitive genes shown in Tables 2, 3, 4         and 5 is taken to mean the subject is pre-disposed to         Alzheimer's disease.

In certain embodiments of the invention, the difference may be measured as an increase in the expression level of one or more of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5, and/or the activity of one or more of the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 as compared with reference/control values and such increase is taken to mean the subject is pre-disposed to Alzheimer's disease. Such “pre-disposition to Alzheimer's disease” may be manifest as an increased lifetime risk of developing Alzheimer's disease as compared with the average lifetime risk associated with the general population, and/or as an earlier age of onset of Alzheimer's disease in affected individuals.

As described above in connection with the diagnostic methods aspect of the invention, the presently-claimed methods comprise as a first step measuring either the expression level of one or more of the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5 and/or the activity of one or more of the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5. Gene expression may be analysed by assessing levels of mRNA produced following gene transcription or by assessing levels of the protein produced following translation of the mRNA. The detection of mRNA and protein levels may be carried out by methods known to those skilled in the art. Protein activity may also be analysed using suitable assays known to those skilled in the art.

In certain embodiments of the invention, protein activity may be measured directly. For example, the activity of a kinase enzyme may be measured using an assay that detects phosphorylation of the enzyme's direct substrate. Protein activity may also be measured indirectly by measuring alterations and/or changes in the level and/or activity of metabolites linked to the activity of the proteins encoded by the rapamycin-sensitive genes shown in Tables 2, 3, 4 and 5.

As a second step, the methods require a comparison between the gene expression levels and/or protein activity measured in the first step and the gene expression levels and/or protein activity defined as reference or control values. Such reference or control values may be determined from measurements made using age-matched healthy subjects, preferably wherein such subjects exhibit no signs of cognitive impairment. Alternatively or in addition, such reference or control values may be determined from measurements made using subjects that are known not to have developed Alzheimer's disease during their lifetime.

The screening methods described herein will typically be used to assess the pre-disposition to Alzheimer's disease in individuals that are otherwise asymptomatic for this disease.

Methods of Assessing Pre-Disposition to Alzheimer's Disease Based on Detection of Polymorphisms

In a further aspect, provided herein is a method of screening a human subject for pre-disposition to Alzheimer's disease, which method comprises genotyping the subject for a polymorphism in one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

In this aspect of the invention, “a polymorphism” can be taken to mean one or more polymorphisms. Therefore, provided herein is a method of screening a human subject for pre-disposition to Alzheimer's disease, which method comprises genotyping the subject for one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

In a still further aspect, provided herein is a method of screening a human subject for pre-disposition to Alzheimer's disease, which method comprises genotyping the subject for one or more polymorphisms in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

As used herein, the term “polymorphism” includes single nucleotide polymorphisms or SNPs, which are changes in which a single base in the DNA differs from the usual base at that position. Millions of SNPs have been catalogued throughout the human genome, and many of these have been linked to increased or decreased susceptibility or pre-disposition to certain diseases. SNPs found within the ApoE gene have already been linked to elevated risk of Alzheimer's disease.

Associations between polymorphisms or polymorphic variants and susceptibility to Alzheimer's disease can be identified or confirmed by carrying out genetic association studies, for example family-based or case-control association studies. Associations may also be determined by evaluating the relationship between deregulated gene expression seen in the brain of Alzheimer's disease patients and the underlying genotype.

In the present methods for screening for pre-disposition to Alzheimer's disease, a subject is genotyped for one or more polymorphisms or polymorphic variants in one or more of the rapamycin-sensitive genes shown in Table 1. In certain embodiments, the subject may be genotyped for two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms or polymorphic variants in one or more of the rapamycin-sensitive genes shown in Table 1. Wherein the methods involve genotyping for more than one polymorphism, the polymorphisms may be in the same rapamycin-sensitive gene or in different rapamycin-sensitive genes.

Alternatively, or in addition, the subject may be genoytyped for one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms or polymorphic variants in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1. Wherein the methods involve genotyping for more than one polymorphism, the polymorphisms may be in the same gene or in different genes. Polymorphisms or polymorphic variants in genes which affect the expression of rapamycin-sensitive genes may be located in genes encoding regulators, particularly upstream regulators, of expression of genes in the mTOR signalling pathway described herein.

In the context of the present invention, a polymorphism “in” a gene should be taken to mean a genetic variant present at any position within the full-length native gene. Polymorphisms may therefore be located in exons, introns or in regulatory regions located upstream or downstream of the coding segment.

In preferred embodiments, the method comprises genotyping a subject for one or more polymorphisms in one or more rapamycin-sensitive genes selected from LILRB2, FAM5C, CRP, CLU, FCGR2A, CD1E, FAM5C, LPL, SYK and CUX1. Alternatively, or in addition, the method may comprise genotyping a subject for one or more polymorphisms in one or more genes which affect the expression of one or more rapamycin-sensitive genes, wherein the “regulatory” genes are selected from POU2F1, ADRA1A, PRDM1 and LOXL2.

POU2F1 is a transcriptional regulator of the mTOR genes: A2M, CRP, CSF1R, CYP2C9, ESR1, GSTM3, IL2, IL6, PRKAA2, SPP1, TLR4 from Table 1. ADRA1A is a regulator of mTOR regulated genes: CDKN1B, EGR1, FGF7, FN1, IL6, JUN, LOX, NR4A1, NR4A2 from Table 1. LOXL2 is an upstream regulator of mTOR regulated genes: CDH1, FN1, MMP9 from Table 1. PRDM1 is the upstream regulator of mTOR regulated genes: ESR1, IGHG1, IL10, IL2, IL6, MYC, RELN, SCGN from Table 1.

In preferred embodiments, the screening methods involve genotyping a subject for one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of single nucleotide polymorphisms consisting of rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214, as characterised in Table 14. The presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease. The bases of the variant alleles associated with Alzheimer's disease for the SNPs described above are as follows: rs798893 (C), rs725106 (A), rs1341665 (A), rs1359059 (A), rs1532278 (C), rs1801274 (G), rs2036108 (T), rs811925 (G), rs883524 (C), rs1065457 (G), rs1148613 (C), rs295 (C), rs290258 (G), rs365836 (G) and rs569214 (T) (see Table 14).

The screening methods may also involve genotyping a subject for one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of polymorphisms consisting of polymorphisms, particularly SNPs, associated with or in linkage disequilibrium (LD) with the single nucleotide polymorphisms: rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214. Polymorphisms “associated” with the SNPs characterised in Table 14 include polymorphisms in close proximity to the identified SNPs. Polymorphisms in linkage disequilibrium with the characterised SNPs could be identified by one of skill in the art using standard association mapping techniques described in the art.

The screening methods of the present invention may be carried out in conjunction with other screening methods used to assess pre-disposition to Alzheimer's disease including use of screening methods based on measuring the expression of the rapamycin-sensitive gene targets described elsewhere herein (see Tables 2-5). Other methods for assessing a subject's pre-disposition or risk of Alzheimer's disease may utilise other known risk factors, including in particular environmental risk factors such as plasma homocysteine levels.

In accordance with the invention, genotyping of polymorphic variants can be carried out using any suitable methodology known in the art and it is to be understood that the invention is in no way limited by the precise technique used to carry out the genotyping.

Known techniques which may be used for genotyping single nucleotide polymorphisms include ligation detection reaction (LDR; Day, D. J., Speiser, P. W., White, P. C. & Barany, F. Genomics 29, 152 62 (1995)), mass spectrometry, particularly matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS), single nucleotide primer extension and DNA chips or microarrays (see review by Schafer, A. J. and Hawkins, J. R. in Nature Biotechnology, Vol 16, pp 33-39 (1998)). The use of DNA chips or microarrays may enable simultaneous genotyping at many different polymorphic loci in a single individual or the simultaneous genotyping of a single polymorphic locus in multiple individuals. SNPs may also be scored by DNA sequencing.

In addition to the above, SNPs are commonly scored using PCR-based techniques, such as PCR-SSP using allele-specific primers (described by Bunce M, et al., Tissue Antigens, 1995; 50: 23-31). This method generally involves performing DNA amplification reactions using genomic DNA as the template and two different primer pairs, the first primer pair comprising an allele-specific primer which under appropriate conditions is capable of hybridising selectively to the wild type allele and a non allele-specific primer which binds to a complementary sequence elsewhere within the gene in question, the second primer pair comprising an allele-specific primer which under appropriate conditions is capable of hybridising selectively to the variant allele and the same non allele-specific primer. Further suitable techniques for scoring SNPs include PCR ELISA and denaturing high performance liquid chromatography (DHPLC).

If the SNP results in the abolition or creation of a restriction site, genotyping can be carried out by performing PCR using non-allele specific primers spanning the polymorphic site and digesting the resultant PCR product using the appropriate restriction enzyme (also known as PCR-RFLP). Restriction fragment length polymorphisms, including those resulting from the presence of a single nucleotide polymorphism, may be scored by digesting genomic DNA with an appropriate enzyme then performing a Southern blot using a labelled probe corresponding to the polymorphic region (see Molecular Cloning: A Laboratory Manual, Sambrook, Fritsch and Maniatis, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.).

In the context of the present invention, “genotyping” of any given polymorphic variant may advantageously comprise screening for the presence or absence in the genome of the subject of both the normal or wild type allele and the variant or mutant allele associated with disease, or may comprise screening for the presence or absence of either individual allele, it generally being possible to draw conclusions about the genotype of an individual at a polymorphic locus having two alternative allelic forms just by screening for one or other of the specific alleles.

Alzheimer's disease is a complex and multi-factorial condition. In any given individual the development of AD is likely to be associated with accumulation of genetic variation within a single gene, or across multiple genes, and the accumulated variants may have an additive effect. In view of the foregoing, it is within the scope of the invention to perform genotyping of polymorphisms or polymorphic variants within multiple genes, wherein at least one of the genes is selected from the rapamycin-sensitive genes shown in Table 1. Such a “panel screen” of multiple genes may be used to simultaneously analyse multiple polymorphisms that serve as markers of susceptibility/pre-disposition to Alzheimer's disease in the same human subject. In a preferred embodiment, genotyping of multiple polymorphisms in a single patient sample may be carried out simultaneously, for example with the use of a microarray or “gene chip”.

In certain embodiments of the invention, the screening for pre-disposition to Alzheimer's disease will involve genotyping a subject for multiple polymorphisms or polymorphic variants in one or more of the genes shown in Table 1 or multiple polymorphisms or polymorphic variants in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, or a combination of both. In the context of the present invention, “multiple” should be taken to mean two or more, three or more, four or more, five or more, six or more etc. The presence of multiple variant alleles associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease.

In further preferred embodiments, the screening methods will involve genotyping a subject for a combination of single polynucleotide polymorphisms selected from the following:

-   -   (i) rs1065457, rs798893 and rs2036108;     -   (ii) rs1065457, rs1148613, rs290258, rs725106 and rs1341665;     -   (iii) rs1065457, rs295, rs1359059, rs1532278, rs798893,         rs365836, rs725106 and rs1341665;     -   (iv) rs1148613, rs290258, rs725106, rs1341665 and rs2036108;     -   (v) rs1065457, rs1148613, rs290258, rs725106, rs1341665 and         rs2036108;     -   (vi) rs1065457, rs1359059, rs725106 and rs2036108; or     -   (vii) rs798893 and rs725106,         wherein the presence of a combination of variant alleles         associated with Alzheimer's disease is an indication that the         subject is predisposed to Alzheimer's disease. The variant         alleles associated with Alzheimer's disease for each of the SNPs         in the combinations described above are as follows: rs798893         (C), rs725106 (A), rs1341665 (A), rs1359059 (A), rs1532278 (C),         rs1801274 (G), rs2036108 (T), rs811925 (G), rs883524 (C),         rs1065457 (G), rs1148613 (C), rs295 (C), rs290258 (G),         rs365836 (G) and rs569214 (T).

Genotyping is preferably carried out in vitro, and is most preferably performed on an isolated sample containing genomic DNA prepared from a suitable tissue sample obtained from the subject under test. Most commonly, genomic DNA is prepared from a sample of whole blood or brain tissue, according to standard procedures which are well known in the art. If genomic sequence data for the individual under test in the region containing the SNP is available, for example in a genomic sequence database as a result of a prior genomic sequencing exercise, then genotyping of the SNP may be accomplished by searching the available sequence data.

In the case of genetic variants which have a detectable effect on the mRNA transcripts transcribed from a given gene, for example variants which cause altered splicing or which affect transcript termination or which affect the level or mRNA expression, then as an alternative to detecting the presence of the variant at the genomic DNA level, the presence of the variant may be inferred by evaluating the mRNA expression pattern using any suitable technique. Similarly, in the case of genetic variants which have a detectable effect on the protein products encoded by a gene, for example variants which cause a change in primary amino acid sequence, structure or properties of the encoded protein, the presence of the variant may be inferred by evaluating the sequence, structure or properties of the protein using any convenient technique.

The above-described screening methods may be used prognostically to identify individuals pre-disposed to Alzheimer's disease (AD) by virtue of their genetic make-up. The “pre-disposition to Alzheimer's disease” may be manifest as an increased risk of developing disease as compared to the general population, or as an earlier age of disease onset as compared to individuals who do not possess a variant allele associated with Alzheimer's disease.

In certain embodiments, the method may be used to screen asymptomatic individuals (i.e. individuals who do not exhibit significant symptoms of AD according to standard diagnostic criteria) in order to identify those “at risk” of developing AD, and/or those likely to exhibit an earlier age of onset of AD. The results of such screens may facilitate early intervention with therapeutic treatments, particularly prophylactic treatments aimed at preventing, reducing or delaying the clinical symptoms of Alzheimer's disease.

In further embodiments the screening methods may be used to screen patients who exhibit clinical symptoms of Alzheimer's disease, for example to assist in correct diagnosis of AD and/or to investigate the genetic basis of suspected or confirmed AD.

Diagnostic Methods Based on Detection of Polymorphisms

In a further aspect, the invention provides a method to assist with diagnosis of Alzheimer's disease in a live human subject, which method comprises genotyping the subject for a polymorphism in one or more of the rapamycin-sensitive genes shown in Table 1, or a polymorphism in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with Alzheimer's disease is indicative of Alzheimer's disease.

Embodiments of the invention described in the context of diagnostic methods of the invention based on measuring the expression level of one or more rapamycin-sensitive genes are equally applicable to this further aspect of the invention. In addition, embodiments of the invention described in the context of methods for assessing pre-disposition to Alzheimer's disease based on genotyping a subject for one or more polymorphisms are equally applicable to this further aspect of the invention.

Methods to assist with diagnosis of Alzheimer's disease in a live human subject have been described in International patent application no. WO02/073212, incorporated herein by reference. These methods comprise a step of screening non-neuronal cells from a human subject for the presence of a cell cycle regulatory defect at the G1/S transition. One of the ways in which this defect can be assessed is by measuring the responsiveness of the non-neuronal cells to a G1 inhibitor, for example rapamycin. Differential responsiveness to a G1 inhibitor in lymphocytes taken from a subject suspected of having Alzheimer's disease is indicative of disease.

The diagnostic test described in WO02/073212 was developed based on the discovery that Alzheimer's disease is associated with aberrant re-entry of neurons into the cell division cycle. This change is an early event in disease pathogenesis preceding formation of both amyloid-β plaques and neurofibrillary tangles. Therefore, detection of these cell cycle changes may be used to assist with diagnosis of Alzheimer's disease at an early stage, even in asymptomatic individuals.

Previous studies have shown that it is not cell cycle re-entry per se that contributes to Alzheimer's disease but rather the inability of neurons from Alzheimer's disease patients to respond appropriately to this cell-cycle re-entry. In particular, neurons from Alzheimer's disease patients are unable to initiate G1 arrest and subsequently undergo re-differentiation, as a result of a defect in the G1/S regulatory checkpoint. Furthermore, this regulatory defect at the G1/S transition occurs in cells other than neurons in individuals with Alzheimer's disease, for example lymphocytes.

It is therefore possible to assist with the diagnosis of Alzheimer's disease in the live human subject by measuring the differential responsiveness of lymphocytes taken from the subject to G1 inhibitors, such as rapamycin.

The present diagnostic methods are based on the genotyping of a subject to look for the presence of polymorphisms, particularly single nucleotide polymorphisms (SNPs) in rapamycin-sensitive genes or in genes which affect the expression of rapamycin-sensitive genes. Importantly, it has been shown that SNPs within rapamycin-sensitive genes or SNPs in genes which affect the expression of rapamycin-sensitive genes correlate with the differential response to rapamycin observed in lymphocytes collected from individual Alzheimer's disease patients. Therefore, the present methods involve genotyping a subject for a polymorphism in one or more of the rapamycin-sensitive genes shown in Table 1, or a polymorphism in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1 as an independent means to assist with diagnosis of Alzheimer's disease. In certain embodiments, the methods may involve genotyping a subject for multiple polymorphisms or polymorphic variants in one or more of the genes shown in Table 1 or multiple polymorphisms or polymorphic variants in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, or a combination of both. In a preferred embodiment, genotyping of multiple polymorphisms in a single patient sample may be carried out simultaneously, for example with the use of a microarray or “gene chip”.

In preferred embodiments, the method comprises genotyping a subject for one or more polymorphisms in one or more rapamycin-sensitive genes selected from LILRB2, FAM5C, CRP, CLU, FCGR2A, CD1E, FAM5C, LPL, SYK and CUX1. Alternatively, or in addition, the method may comprise genotyping a subject for one or more polymorphisms in one or more genes which affect the expression of one or more rapamycin-sensitive genes, wherein the “regulatory” genes are selected from POU2F1, ADRA1A, PRDM1 and LOXL2.

In preferred embodiments, the diagnostic methods involve genotyping a subject for one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of single nucleotide polymorphisms consisting of rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214, as characterised in Table 14. The presence of at least one variant allele associated with Alzheimer's disease is an indication that the subject is pre-disposed to Alzheimer's disease. The variant alleles associated with Alzheimer's disease for the SNPs described above are as follows: rs798893 (C), rs725106 (A), rs1341665 (A), rs1359059 (A), rs1532278 (C), rs1801274 (G), rs2036108 (T), rs811925 (G), rs883524 (C), rs1065457 (G), rs1148613 (C), rs295 (C), rs290258 (G), rs365836 (G) and rs569214 (T).

The screening methods may also involve genotyping a subject for one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of polymorphisms consisting of polymorphisms, particularly SNPs, associated with or in linkage disequilibrium (LD) with the single nucleotide polymorphisms: rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214. Polymorphisms “associated” with the SNPs in Table 14 include polymorphisms in close proximity to the characterised SNPs. Polymorphisms in linkage disequilibrium with the characterised SNPs could be identified by one of skill in the art using standard association mapping techniques described in the art.

In further preferred embodiments, the diagnostic methods will involve genotyping a subject for a combination of single polynucleotide polymorphisms selected from the following:

-   -   (i) rs1065457, rs798893 and rs2036108;     -   (ii) rs1065457, rs1148613, rs290258, rs725106 and rs1341665;     -   (iii) rs1065457, rs295, rs1359059, rs1532278, rs798893,         rs365836, rs725106 and rs1341665;     -   (iv) rs1148613, rs290258, rs725106, rs1341665 and rs2036108;     -   (v) rs1065457, rs1148613, rs290258, rs725106, rs1341665 and         rs2036108;     -   (vi) rs1065457, rs1359059, rs725106 and rs2036108; or     -   (vii) rs798893 and rs725106,         wherein the presence of a combination of variant alleles         associated with Alzheimer's disease is indicative of a positive         Alzheimer's disease diagnosis.

As noted above, the diagnostic methods described herein may also be used in combination or together with other methods or tests used for Alzheimer's disease diagnosis, for example in order to improve the specificity and/or sensitivity of these methods or tests. In a preferred embodiment, the diagnostic method of the present invention involves a first step of genotyping a subject for a combination of polymorphisms consisting of pr1 and pr10 and a second step of determining plasma homocysteine levels in the same subject.

Arrays and Kits

The present invention also provides arrays and kits for detecting one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more genetic polymorphisms or polymorphic variants in a sample taken from a subject. The one or more polymorphisms to be detected by the arrays and kits provided herein are in one or more of the rapamycin-sensitive genes shown in Table 1, or in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1.

Embodiments of the invention already described above in relation to the screening methods and diagnostic methods of the invention relating to the use of polymorphisms are equally applicable to the arrays and kits provided.

The sample taken from the subject may be any sample suitable for genetic analysis including but not limited to blood, saliva, tears, urine, skin, hair or any other tissue containing nucleic acid.

The array or kit may take any suitable format for the detection of polymorphisms, and the reagents forming the array or included in the kit will be dependent on the format adopted by the user. In certain embodiments, the array may take the form of a microarray or “gene chip” wherein oligonucleotides capable of detecting the one or more polymorphisms of interest, if present within the sample, are immobilised on a solid substrate. In certain embodiments, the oligonucleotides are allele-specific oligonucleotides capable of detecting the one or more polymorphisms by hybridisation to the variant allele. The invention therefore provides an array comprising multiple allele-specific oligonucleotides capable of detecting at least two, at least three, at least four, at least five etc different polymorphisms as described elsewhere herein. The design of suitable allele-specific oligonucleotides or probes and the construction of arrays comprising allele-specific oligonucleotides for detecting one or more polymorphisms, particularly SNPs, in a sample could be carried out using standard techniques well known in the art.

Kits according to the present invention may include reagents suitable for carrying out allele-specific Q-PCR, in order to detect one or more polymorphisms. Allele-specific Q-PCR is a variation of the standard polymerase chain reaction, which can be used to identify SNPs in a sample containing nucleic acid. The reagents would include all standard PCR reagents (DNA polymerase, Tris-HCl, (NH₄)₂SO₄, MgCl₂, Tween20, dATP, dCTP, dTTP, dGTP) and suitable primers with 3′ ends encompassing the SNP. Kits may also include allele-specific restriction enzymes, which can be used to detect the presence of SNPs based on the digestion pattern produced when the restriction enzyme digests the nucleic acid sample, as described elsewhere herein.

Methods to Monitor mTOR Signalling

As discussed elsewhere herein, the polymorphisms to be detected in the context of the screening and diagnostic methods described above, are either in one or more of the rapamycin-sensitive genes shown in Table 1, or in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1. The inhibitor rapamycin is known to inhibit the serine/threonine kinase mTOR in human cells and thereby reduce signalling downstream of this protein. It follows therefore that genes identified as rapamycin-sensitive genes are linked to mTOR signalling in cells.

Therefore, in a further aspect, the present invention also provides a method by which to monitor mTOR signalling in a human cell, which method comprises detecting one or more polymorphisms in one or more of the rapamycin-sensitive genes shown in Table 1, or one or more polymorphisms in one or more genes which affect the expression of one or more of the rapamycin-sensitive genes shown in Table 1, wherein the presence of at least one variant allele associated with a differential response to rapamycin is indicative of the status of mTOR signalling in the cell.

The cytoplasmic kinase mTOR is stimulated or activated by a wide variety of upstream signals. These include signals generated or triggered as a result of nutrient sensing, hypoxia, and/or the activity of growth factors and their cognate receptors. Activation of mTOR upregulates its kinase activity and thereby increases mTOR-mediated phosphorylation of downstream protein targets within the cell. In most cases, the direct downstream protein targets of mTOR interact with a variety of further molecular targets, and in doing so, stimulate a wide variety of cellular responses, such as increased protein synthesis and the promotion of cell growth and proliferation. The chain of molecular events triggered downstream of mTOR-mediated phosphorylation of its direct protein targets is defined herein as the “mTOR signalling pathway”.

The methods of the present aspect of the invention allow for the monitoring of mTOR signalling. By “monitoring” is meant determination of the level of activity downstream of the mTOR kinase, for example the level of activity of proteins present within the downstream signalling pathways. Monitoring may be carried out in particular, to determine the functional integrity of the mTOR signalling pathway within a human cell.

In preferred embodiments, the one or more polymorphisms for detection are in one or more of the rapamycin-sensitive genes selected from LILRB2, FAM5C, CRP, CLU, FCGR2A, CD1E, FAM5C, LPL, SYK and CUX1 and/or in one or more of the genes which affect the expression of one or more rapamycin-sensitive genes, selected from POU2F1, ADRA1A, PRDM1 and LOXL2.

In preferred embodiments, the methods involve detecting one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of single nucleotide polymorphisms consisting of rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214, as characterised in Table 14. The methods may also involve detecting one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more polymorphisms selected from the group of polymorphisms consisting of polymorphisms, particularly SNPs, associated with or in linkage disequilibrium (LD) with the single nucleotide polymorphisms: rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214.

As described elsewhere herein, cells from subjects with Alzheimer's disease typically exhibit a differential response to G1/S inhibitors, including rapamycin, as a result of a defect in the G1/S cell cycle transition. This differential response is reported in for example, WO02/073212, incorporated herein by reference. The SNPs or variant alleles characterised herein are associated with a differential response to rapamycin as seen in lymphocytes collected from individuals with Alzheimer's disease. As noted above, rapamycin responsiveness is indicative of the status of mTOR signalling in the cell wherein “status” should be taken to mean the functional integrity of signalling through the mTOR signalling pathway. Therefore, the presence of at least one variant allele associated with a differential response to rapamycin may be used to determine the status of mTOR signalling in a cell. In certain embodiments, the presence of at least one variant allele associated with a differential response to rapamycin may be used to determine that the functional integrity of the mTOR signalling pathway is compromised in a particular cell.

Wherein the one or more polymorphisms is/are selected from the group consisting of rs798893, rs725106, rs1341665, rs1359059, rs1532278, rs1801274, rs2036108, rs811925, rs883524, rs1065457, rs1148613, rs295, rs290258, rs365836 and rs569214, the bases of the variant alleles associated with a differential response to rapamycin are as follows: rs798893 (C), rs725106 (A), rs1341665 (A), rs1359059 (A), rs1532278 (C), rs1801274 (G), rs2036108 (T), rs811925 (G), rs883524 (C), rs1065457 (G), rs1148613 (C), rs295 (C), rs290258 (G), rs365836 (G) and rs569214 (T).

The methods of the present invention may be used to monitor mTOR signalling in any type of human cell. For example, the human cell may be a cell pre-treated with a compound such as a pharmacological inhibitor. In a preferred embodiment of the invention, the human cell is a lymphocyte.

Furthermore, in preferred embodiments of the invention, the human cell may be taken from an individual or human subject suspected of having a particular condition or disease, or considered to be at risk of developing a particular disease, most preferably Alzheimer's disease. Wherein the human subject is suspected of having or developing Alzheimer's disease, the cell may be taken from a subject that is asymptomatic for Alzheimer's disease, or a subject who exhibits mild cognitive impairment or a subject exhibiting one or more symptoms consistent with Alzheimer's disease.

The purpose of monitoring mTOR signalling in a cell taken from an individual or subject suspected of having a particular disease or considered at risk of a particular disease, may be to assist with diagnosis of disease in the subject or to assess the subject's pre-disposition to disease. In the preferred embodiment of the present invention wherein the human cell is isolated from a human subject suspected of having Alzheimer's disease, the method may be carried out in order to assist with the diagnosis of Alzheimer's disease or to assess a subject's pre-disposition to Alzheimer's disease.

The present methods may also be used to assist with diagnosis of other diseases or conditions wherein dysregulation of signalling through the mTOR pathway is an underlying cause or consequence, for example cancer, type II diabetes, dementia following brain injury or stroke.

TABLE 1 Rapamycin-sensitive genes (1051 genes) Symbol Entrez Gene Name Location Type(s) A2M alpha-2-macroglobulin Extracellular Space transporter AADACL2 arylacetamide deacetylase-like 2 unknown other AASDH aminoadipate-semialdehyde dehydrogenase unknown enzyme ABCA8 ATP-binding cassette, sub-family A (ABC1), member 8 Plasma Membrane transporter ABCB5 ATP-binding cassette, sub-family B (MDR/TAP), Plasma Membrane transporter member 5 ABCD2 ATP-binding cassette, sub-family D (ALD), member 2 Cytoplasm transporter ABHD2 abhydrolase domain containing 2 unknown enzyme ABI3BP ABI family, member 3 (NESH) binding protein Extracellular Space other ABLIM2 actin binding LIM protein family, member 2 Cytoplasm other ABRA actin-binding Rho activating protein Cytoplasm transcription regulator ABTB1 ankyrin repeat and BTB (POZ) domain containing 1 Cytoplasm translation regulator ACOX2 acyl-CoA oxidase 2, branched chain Cytoplasm enzyme ACPP acid phosphatase, prostate Extracellular Space phosphatase ACSL6 acyl-CoA synthetase long-chain family member 6 Cytoplasm enzyme ACSS1 acyl-CoA synthetase short-chain family member 1 Cytoplasm enzyme ACTRT1 actin-related protein T1 Cytoplasm other ACVR2B activin A receptor, type IIB Plasma Membrane kinase ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 13 ADAMTS15 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 15 ADAMTS16 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space other motif, 16 ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 2 ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 20 ADAMTS3 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 3 ADAMTS9 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase motif, 9 ADAMTSL3 ADAMTS-like 3 unknown other ADAMTSL4 ADAMTS-like 4 Extracellular Space other ADAMTSL5 ADAMTS-like 5 Extracellular Space other ADH6 (includes EG: 130) alcohol dehydrogenase 6 (class V) Cytoplasm enzyme ADIPOQ adiponectin, C1Q and collagen domain containing Extracellular Space other ADSSL1 adenylosuccinate synthase like 1 Cytoplasm enzyme AGT angiotensinogen (serpin peptidase inhibitor, clade A, Extracellular Space growth factor member 8) AGTR1 angiotensin II receptor, type 1 Plasma Membrane G-protein coupled receptor AHNAK AHNAK nucleoprotein Nucleus other AHNAK2 AHNAK nucleoprotein 2 unknown other AKR1D1 aldo-keto reductase family 1, member D1 (delta 4-3- Cytoplasm enzyme ketosteroid-5-beta-reductase) ALDH1A3 aldehyde dehydrogenase 1 family, member A3 Cytoplasm enzyme AMY1A (includes others) amylase, alpha 1A (salivary) Extracellular Space enzyme ANGPT2 angiopoietin 2 Extracellular Space growth factor ANGPTL2 angiopoietin-like 2 Extracellular Space other ANGPTL5 angiopoietin-like 5 Extracellular Space other ANK1 ankyrin 1, erythrocytic Plasma Membrane other ANKRD12 ankyrin repeat domain 12 Nucleus other ANKRD36B (includes ankyrin repeat domain 36B Nucleus transcription others) regulator ANKRD36B (includes ankyrin repeat domain 36B Nucleus transcription others) regulator ANKRD42 ankyrin repeat domain 42 Nucleus transcription regulator ANKRD45 ankyrin repeat domain 45 Nucleus transcription regulator ANKRD50 ankyrin repeat domain 50 unknown other ANKRD6 ankyrin repeat domain 6 Nucleus transcription regulator ANKS1B ankyrin repeat and sterile alpha motif domain Nucleus other containing 1B ANO3 anoctamin 3 unknown other ANXA10 annexin A10 Cytoplasm other ANXA2R annexin A2 receptor Plasma Membrane other AP1S1 adaptor-related protein complex 1, sigma 1 subunit Cytoplasm transporter APBB1IP amyloid beta (A4) precursor protein-binding, family B, Cytoplasm other member 1 interacting protein APOB apolipoprotein B (including Ag(x) antigen) Extracellular Space transporter APOBEC3G apolipoprotein B mRNA editing enzyme, catalytic Nucleus enzyme polypeptide-like 3G APOLD1 apolipoprotein L domain containing 1 unknown other AQP12A/AQP12B aquaporin 12B Cytoplasm transporter AQP4 aquaporin 4 Plasma Membrane transporter AQP9 aquaporin 9 Plasma Membrane transporter AR androgen receptor Nucleus ligand- dependent nuclear receptor ARHGAP28 Rho GTPase activating protein 28 Cytoplasm other ARHGEF4 Rho guanine nucleotide exchange factor (GEF) 4 Cytoplasm other ARHGEF6 Rac/Cdc42 guanine nucleotide exchange factor Cytoplasm other (GEF) 6 ARL14 ADP-ribosylation factor-like 14 unknown other ARL17B/LOC100294341 ADP-ribosylation factor-like 17B unknown other ARMC2 armadillo repeat containing 2 unknown other ARSE arylsulfatase E (chondrodysplasia punctata 1) Cytoplasm enzyme AS3MT arsenic (+3 oxidation state) methyltransferase Cytoplasm enzyme ASB11 ankyrin repeat and SOCS box containing 11 Nucleus transcription regulator ASPM asp (abnormal spindle) homolog, microcephaly Nucleus other associated (Drosophila) ASXL3 additional sex combs like 3 (Drosophila) unknown other ATAD3A/ATAD3B ATPase family, AAA domain containing 3A Nucleus other ATF7IP activating transcription factor 7 interacting protein Nucleus transcription regulator ATP13A4 ATPase type 13A4 unknown transporter ATP6V0D2 ATPase, H+ transporting, lysosomal 38 kDa, V0 Cytoplasm transporter subunit d2 ATP8B3 ATPase, aminophospholipid transporter, class I, type Cytoplasm transporter 8B, member 3 ATRNL1 attractin-like 1 unknown other AUTS2 autism susceptibility candidate 2 unknown other B2M beta-2-microglobulin Plasma Membrane transmembrane receptor B3GALT4 UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, Cytoplasm enzyme polypeptide 4 B4GALT6 UDP-Gal:betaGlcNAc beta 1,4- Cytoplasm enzyme galactosyltransferase, polypeptide 6 BAIAP2 BAI1-associated protein 2 Plasma Membrane kinase BAIAP2L2 BAI1-associated protein 2-like 2 Cytoplasm other BARX2 BARX homeobox 2 Nucleus transcription regulator BCCIP BRCA2 and CDKN1A interacting protein Nucleus other BCL2 B-cell CLL/lymphoma 2 Cytoplasm transporter BEGAIN brain-enriched guanylate kinase-associated homolog Nucleus other (rat) BEND2 BEN domain containing 2 unknown other BEND6 BEN domain containing 6 unknown other BEST3 bestrophin 3 Nucleus ion channel BMP7 bone morphogenetic protein 7 Extracellular Space growth factor BMX BMX non-receptor tyrosine kinase Cytoplasm kinase BNC1 basonuclin 1 Nucleus transcription regulator BPESC1 blepharophimosis, epicanthus inversus and ptosis, unknown other candidate 1 (non-protein coding) BPI bactericidal/permeability-increasing protein Plasma Membrane transporter BPIFB1 BPI fold containing family B, member 1 Extracellular Space other BRIP1 BRCA1 interacting protein C-terminal helicase 1 Nucleus enzyme BSN bassoon (presynaptic cytomatrix protein) Plasma Membrane other BSND Bartter syndrome, infantile, with sensorineural Plasma Membrane ion channel deafness (Barttin) BSPRY B-box and SPRY domain containing Cytoplasm other BTNL9 butyrophilin-like 9 unknown other BVES blood vessel epicardial substance Plasma Membrane other C10orf10 chromosome 10 open reading frame 10 Cytoplasm other C10orf107 chromosome 10 open reading frame 107 unknown other C10orf111 chromosome 10 open reading frame 111 unknown other C11orf67 chromosome 11 open reading frame 67 unknown other C11orf87 chromosome 11 open reading frame 87 unknown other C11orf88 chromosome 11 open reading frame 88 unknown other C12orf42 chromosome 12 open reading frame 42 unknown other C15orf43 chromosome 15 open reading frame 43 unknown other C15orf48 chromosome 15 open reading frame 48 Nucleus other C17orf78 chromosome 17 open reading frame 78 unknown other C17orf99 chromosome 17 open reading frame 99 unknown other C18orf26 chromosome 18 open reading frame 26 unknown other C1orf110 chromosome 1 open reading frame 110 unknown other C1orf127 chromosome 1 open reading frame 127 unknown other C1orf173 chromosome 1 open reading frame 173 unknown other C1orf226 chromosome 1 open reading frame 226 unknown other C1orf87 chromosome 1 open reading frame 87 unknown other C1QTNF6 C1q and tumor necrosis factor related protein 6 Extracellular Space other C20orf132 chromosome 20 open reading frame 132 unknown other C20orf85 chromosome 20 open reading frame 85 unknown other C2orf16 chromosome 2 open reading frame 16 unknown other C3orf36 chromosome 3 open reading frame 36 unknown other C3orf70 chromosome 3 open reading frame 70 unknown other C4orf19 chromosome 4 open reading frame 19 unknown other C4orf22 chromosome 4 open reading frame 22 unknown other C4orf26 chromosome 4 open reading frame 26 unknown other C4orf36 chromosome 4 open reading frame 36 unknown other C6orf223 chromosome 6 open reading frame 223 unknown other C7orf41 chromosome 7 open reading frame 41 unknown other C8orf42 chromosome 8 open reading frame 42 unknown other CA12 carbonic anhydrase XII Plasma Membrane enzyme CA6 carbonic anhydrase VI Extracellular Space enzyme CACNA1D calcium channel, voltage-dependent, L type, alpha Plasma Membrane ion channel 1D subunit CADPS Ca++-dependent secretion activator Plasma Membrane other CALD1 caldesmon 1 Cytoplasm other CARD14 caspase recruitment domain family, member 14 Cytoplasm other CATSPER2 cation channel, sperm associated 2 Plasma Membrane ion channel CATSPERD catsper channel auxiliary subunit delta unknown other CAV2 caveolin 2 Plasma Membrane other CBX7 chromobox homolog 7 Nucleus other CC2D2A coiled-coil and C2 domain containing 2A unknown other CCDC141 coiled-coil domain containing 141 unknown other CCDC28A coiled-coil domain containing 28A unknown other CCDC34 coiled-coil domain containing 34 unknown other CCDC40 coiled-coil domain containing 40 unknown other CCDC85A coiled-coil domain containing 85A unknown other CCL1 chemokine (C-C motif) ligand 1 Extracellular Space cytokine CCL11 chemokine (C-C motif) ligand 11 Extracellular Space cytokine CCL2 chemokine (C-C motif) ligand 2 Extracellular Space cytokine CCL26 chemokine (C-C motif) ligand 26 Extracellular Space cytokine CCL8 chemokine (C-C motif) ligand 8 Extracellular Space cytokine CCNB2 cyclin B2 Cytoplasm other CCNG2 cyclin G2 Nucleus other CCR1 chemokine (C-C motif) receptor 1 Plasma Membrane G-protein coupled receptor CCR2 chemokine (C-C motif) receptor 2 Plasma Membrane G-protein coupled receptor CD177 CD177 molecule Cytoplasm other CD1A CD1a molecule Plasma Membrane other CD1B CD1b molecule Plasma Membrane other CD1E CD1e molecule Cytoplasm other CD44 (includes CD44 molecule (Indian blood group) Plasma Membrane enzyme EG: 100330801) CD69 CD69 molecule Plasma Membrane transmembrane receptor CD96 CD96 molecule Plasma Membrane other CDC14B CDC14 cell division cycle 14 homolog B (S. cerevisiae) Nucleus phosphatase CDCP1 CUB domain containing protein 1 Plasma Membrane other CDCP2 CUB domain containing protein 2 unknown transporter CDH1 cadherin 1, type 1, E-cadherin (epithelial) Plasma Membrane other CDH13 cadherin 13, H-cadherin (heart) Plasma Membrane other CDH26 cadherin 26 Plasma Membrane other CDH7 cadherin 7, type 2 Plasma Membrane other CDHR1 cadherin-related family member 1 Plasma Membrane other CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1) Nucleus kinase CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2) Nucleus other CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits Nucleus transcription CDK4) regulator CDKN2D cyclin-dependent kinase inhibitor 2D (p19, inhibits Nucleus transcription CDK4) regulator CDON Cdon homolog (mouse) Plasma Membrane other CEACAM1 (includes carcinoembryonic antigen-related cell adhesion Plasma Membrane transmembrane others) molecule 1 (biliary glycoprotein) receptor CELF3 CUGBP, Elav-like family member 3 Nucleus transcription regulator CELF4 CUGBP, Elav-like family member 4 Nucleus translation regulator CELF6 CUGBP, Elav-like family member 6 unknown other CEP68 centrosomal protein 68 kDa Cytoplasm other CFHR5 complement factor H-related 5 Extracellular Space other CFTR cystic fibrosis transmembrane conductance regulator Plasma Membrane ion channel (ATP-binding cassette sub-family C, member 7) CGA glycoprotein hormones, alpha polypeptide Extracellular Space other CGNL1 cingulin-like 1 Plasma Membrane other CHD2 chromodomain helicase DNA binding protein 2 Nucleus enzyme CHP2 calcineurin B homologous protein 2 Cytoplasm other CHRDL2 chordin-like 2 Extracellular Space other CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal) Plasma Membrane transmembrane receptor CKM creatine kinase, muscle Cytoplasm kinase CLC Charcot-Leyden crystal protein Cytoplasm enzyme CLCA2 chloride channel accessory 2 Plasma Membrane ion channel CLEC7A C-type lectin domain family 7, member A Plasma Membrane transmembrane receptor CLTB clathrin, light chain B Plasma Membrane other CLVS1 clavesin 1 Cytoplasm other CNRIP1 cannabinoid receptor interacting protein 1 unknown other CNTN3 contactin 3 (plasmacytoma associated) Plasma Membrane other COBL cordon-bleu homolog (mouse) unknown other COL11A1 collagen, type XI, alpha 1 Extracellular Space other COL13A1 collagen, type XIII, alpha 1 Plasma Membrane other COL1A2 collagen, type I, alpha 2 Extracellular Space other COL6A3 collagen, type VI, alpha 3 Extracellular Space other COL6A6 collagen, type VI, alpha 6 Extracellular Space other COL8A2 collagen, type VIII, alpha 2 Extracellular Space other COMMD6 COMM domain containing 6 unknown other CORIN corin, serine peptidase Plasma Membrane peptidase CORO2A coronin, actin binding protein, 2A Cytoplasm other CPB2 carboxypeptidase B2 (plasma) Extracellular Space peptidase CPE (includes carboxypeptidase E Plasma Membrane peptidase EG: 12876) CPLX2 complexin 2 Cytoplasm other CPXM2 carboxypeptidase X (M14 family), member 2 Extracellular Space peptidase CRB1 crumbs homolog 1 (Drosophila) Plasma Membrane other CREB3L4 cAMP responsive element binding protein 3-like 4 Nucleus transcription regulator CREBRF CREB3 regulatory factor unknown other CRIM1 cysteine rich transmembrane BMP regulator 1 Extracellular Space kinase (chordin-like) CROT carnitine O-octanoyltransferase Cytoplasm enzyme CRP C-reactive protein, pentraxin-related Extracellular Space other CRTAC1 cartilage acidic protein 1 Extracellular Space other CRYBG3 beta-gamma crystallin domain containing 3 unknown other CRYGB crystallin, gamma B Nucleus other CRYGD crystallin, gamma D Cytoplasm other CSDC2 cold shock domain containing C2, RNA binding Cytoplasm other CSF1R colony stimulating factor 1 receptor Plasma Membrane kinase CSN2 casein beta Extracellular Space kinase CTAG1B (includes cancer/testis antigen 1B Cytoplasm other others) CTDSP1 CTD (carboxy-terminal domain, RNA polymerase II, Nucleus phosphatase polypeptide A) small phosphatase 1 CTNNA3 catenin (cadherin-associated protein), alpha 3 Plasma Membrane other CTSF cathepsin F Cytoplasm peptidase CXorf51A/CXorf51B chromosome X open reading frame 51A unknown other CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9 Cytoplasm enzyme CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5 Cytoplasm enzyme CYP4F11 cytochrome P450, family 4, subfamily F, polypeptide Cytoplasm enzyme 11 CYP4F2 cytochrome P450, family 4, subfamily F, polypeptide 2 Cytoplasm enzyme CYP4F3 cytochrome P450, family 4, subfamily F, polypeptide 3 Cytoplasm enzyme CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2 Cytoplasm enzyme CYP4X1 cytochrome P450, family 4, subfamily X, polypeptide 1 Cytoplasm enzyme CYP4Z1 cytochrome P450, family 4, subfamily Z, polypeptide 1 Cytoplasm enzyme CYR61 cysteine-rich, angiogenic inducer, 61 Extracellular Space other CYSLTR2 cysteinyl leukotriene receptor 2 Plasma Membrane G-protein coupled receptor DAOA D-amino acid oxidase activator Cytoplasm other DAPL1 death associated protein-like 1 unknown other DCAF12L1 DDB1 and CUL4 associated factor 12-like 1 unknown other DCC deleted in colorectal carcinoma Plasma Membrane transmembrane receptor DCD dermcidin Extracellular Space other DCLK1 doublecortin-like kinase 1 Plasma Membrane kinase DCN decorin Extracellular Space other DDI1 (includes DNA-damage inducible 1 homolog 1 (S. cerevisiae) unknown other EG: 367012) DDX17 DEAD (Asp-Glu-Ala-Asp) box helicase 17 Nucleus enzyme DEFA4 defensin, alpha 4, corticostatin Extracellular Space other DEFB119 defensin, beta 119 Extracellular Space other DHRS12 dehydrogenase/reductase (SDR family) member 12 Nucleus other DHRS3 dehydrogenase/reductase (SDR family) member 3 Cytoplasm enzyme DKFZP586K1520 DKFZP586K1520 protein unknown other DLEU7 deleted in lymphocytic leukemia, 7 unknown other DLG2 discs, large homolog 2 (Drosophila) Plasma Membrane kinase DLGAP4 discs, large (Drosophila) homolog-associated protein 4 Plasma Membrane other DLX2 distal-less homeobox 2 Nucleus transcription regulator DMRTB1 DMRT-like family B with proline-rich C-terminal, 1 Nucleus transcription regulator DMRTC1/DMRTC1B DMRT-like family C1B unknown other DMRTC2 DMRT-like family C2 Nucleus transcription regulator DNAH1 dynein, axonemal, heavy chain 1 unknown other DNAH6 dynein, axonemal, heavy chain 6 unknown other DNAJB7 DnaJ (Hsp40) homolog, subfamily B, member 7 unknown other DPY19L1P1 dpy-19-like 1 pseudogene 1 (C. elegans) unknown other DRP2 dystrophin related protein 2 Plasma Membrane other DSEL dermatan sulfate epimerase-like unknown enzyme DST dystonin Plasma Membrane other DTD1 D-tyrosyl-tRNA deacylase 1 homolog (S. cerevisiae) Cytoplasm enzyme DUSP13 dual specificity phosphatase 13 Cytoplasm phosphatase DUSP21 dual specificity phosphatase 21 Cytoplasm phosphatase DUSP27 dual specificity phosphatase 27 (putative) unknown phosphatase DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1 Cytoplasm other DYNLRB1 dynein, light chain, roadblock-type 1 Cytoplasm other DZIP1L DAZ interacting protein 1-like unknown other DZIP3 DAZ interacting protein 3, zinc finger Cytoplasm enzyme EBF2 early B-cell factor 2 Nucleus other EBF3 early B-cell factor 3 Nucleus other ECHDC2 enoyl CoA hydratase domain containing 2 unknown other ECM2 (includes extracellular matrix protein 2, female organ and Extracellular Space other EG: 1842) adipocyte specific ECT2L epithelial cell transforming sequence 2 oncogene-like unknown other EDDM3A epididymal protein 3A Extracellular Space other EDDM3B epididymal protein 3B Extracellular Space other EEPD1 endonuclease/exonuclease/phosphatase family unknown other domain containing 1 EFCAB3 EF-hand calcium binding domain 3 unknown other EGF (includes epidermal growth factor Extracellular Space growth factor EG: 13645) EGLN3 egl nine homolog 3 (C. elegans) Cytoplasm enzyme EGR1 early growth response 1 Nucleus transcription regulator ELAVL3 ELAV (embryonic lethal, abnormal vision, Nucleus other Drosophila)-like 3 (Hu antigen C) ELAVL4 ELAV (embryonic lethal, abnormal vision, Cytoplasm other Drosophila)-like 4 (Hu antigen D) ELOVL7 ELOVL fatty acid elongase 7 Cytoplasm enzyme EMCN endomucin Extracellular Space other EMX2OS EMX2 opposite strand/antisense RNA (non-protein unknown other coding) ENPEP glutamyl aminopeptidase (aminopeptidase A) Plasma Membrane peptidase ENPP6 ectonucleotide pyrophosphatase/phosphodiesterase 6 Cytoplasm enzyme ENTPD8 ectonucleoside triphosphate diphosphohydrolase 8 unknown enzyme EPB41L4B erythrocyte membrane protein band 4.1 like 4B unknown transporter EPHA5 EPH receptor A5 Plasma Membrane kinase EPO erythropoietin Extracellular Space cytokine ERBB3 (includes v-erb-b2 erythroblastic leukemia viral oncogene Plasma Membrane kinase EG: 13867) homolog 3 (avian) ERBB4 v-erb-a erythroblastic leukemia viral oncogene Plasma Membrane kinase homolog 4 (avian) ESR1 estrogen receptor 1 Nucleus ligand- dependent nuclear receptor ESYT3 extended synaptotagmin-like protein 3 unknown other EYA1 eyes absent homolog 1 (Drosophila) Nucleus phosphatase F11 coagulation factor XI Extracellular Space peptidase F2 coagulation factor II (thrombin) Extracellular Space peptidase F2RL2 coagulation factor II (thrombin) receptor-like 2 Plasma Membrane G-protein coupled receptor F9 coagulation factor IX Extracellular Space peptidase FAM100B family with sequence similarity 100, member B unknown other FAM135B family with sequence similarity 135, member B unknown enzyme FAM13C family with sequence similarity 13, member C unknown other FAM149B1 family with sequence similarity 149, member B1 unknown other FAM153A/FAM153B family with sequence similarity 153, member A unknown other FAM155A family with sequence similarity 155, member A unknown other FAM162B family with sequence similarity 162, member B unknown other FAM171B family with sequence similarity 171, member B unknown other FAM172A family with sequence similarity 172, member A Cytoplasm transcription regulator FAM177A1 family with sequence similarity 177, member A1 unknown other FAM181B family with sequence similarity 181, member B unknown other FAM19A1 family with sequence similarity 19 (chemokine (C-C unknown other motif)-like), member A1 FAM211A family with sequence similarity 211, member A unknown other FAM24A family with sequence similarity 24, member A unknown other FAM26D family with sequence similarity 26, member D unknown other FAM27E3 (includes family with sequence similarity 27, member E3 unknown other others) FAM43B family with sequence similarity 43, member B unknown other FAM5C family with sequence similarity 5, member C Cytoplasm other FAM64A family with sequence similarity 64, member A Nucleus other FAM71D family with sequence similarity 71, member D unknown other FAM74A3 family with sequence similarity 74, member A3 unknown other FAM84A family with sequence similarity 84, member A unknown other FAM92B family with sequence similarity 92, member B unknown other FAT3 FAT tumor suppressor homolog 3 (Drosophila) unknown other FAXC failed axon connections homolog (Drosophila) unknown other FBLN1 fibulin 1 Extracellular Space other FBN2 (includes fibrillin 2 Extracellular Space other EG: 14119) FBP2 fructose-1,6-bisphosphatase 2 Cytoplasm phosphatase FBXL16 F-box and leucine-rich repeat protein 16 unknown other FCGBP Fc fragment of IgG binding protein Extracellular Space other FGB (includes fibrinogen beta chain Extracellular Space other EG: 110135) FGF11 fibroblast growth factor 11 Extracellular Space growth factor FGF18 fibroblast growth factor 18 Extracellular Space growth factor FGF2 fibroblast growth factor 2 (basic) Extracellular Space growth factor FGF23 fibroblast growth factor 23 Extracellular Space growth factor FGF7 fibroblast growth factor 7 Extracellular Space growth factor FGFR1 fibroblast growth factor receptor 1 Plasma Membrane kinase FGG fibrinogen gamma chain Extracellular Space other FGGY FGGY carbohydrate kinase domain containing unknown other FGR Gardner-Rasheed feline sarcoma viral (v-fgr) Nucleus kinase oncogene homolog FIGN fidgetin Nucleus other FILIP1 filamin A interacting protein 1 Cytoplasm other FJX1 four jointed box 1 (Drosophila) Extracellular Space other FLJ35946 uncharacterized protein FLJ35946 unknown other FLJ36000 uncharacterized FLJ36000 unknown other FLJ37035 uncharacterized LOC399821 unknown other FLJ37644 uncharacterized LOC400618 unknown other FLJ42875 uncharacterized LOC440556 unknown other FMN2 formin 2 unknown other FMO3 flavin containing monooxygenase 3 Cytoplasm enzyme FN1 fibronectin 1 Extracellular Space enzyme FN3K fructosamine 3 kinase Cytoplasm kinase FNBP1 formin binding protein 1 Nucleus enzyme FNDC5 fibronectin type III domain containing 5 unknown other FRAT2 frequently rearranged in advanced T-cell lymphomas 2 Cytoplasm other FREM3 FRAS1 related extracellular matrix 3 Extracellular Space other FRMD4A FERM domain containing 4A Plasma Membrane other FRMD6 FERM domain containing 6 Cytoplasm other FRMD7 FERM domain containing 7 Plasma Membrane other FSTL5 follistatin-like 5 Extracellular Space other FUT9 fucosyltransferase 9 (alpha (1,3) fucosyltransferase) Cytoplasm enzyme G0S2 G0/G1switch 2 Cytoplasm other GAB1 GRB2-associated binding protein 1 Cytoplasm other GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2 Plasma Membrane G-protein coupled receptor GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 Plasma Membrane ion channel GABRA5 gamma-aminobutyric acid (GABA) A receptor, alpha 5 Plasma Membrane ion channel GABRG1 gamma-aminobutyric acid (GABA) A receptor, Plasma Membrane ion channel gamma 1 GABRR2 gamma-aminobutyric acid (GABA) A receptor, rho 2 Plasma Membrane ion channel GAGE1 (includes G antigen 1 unknown other others) GALNT10 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N- Cytoplasm enzyme acetylgalactosaminyltransferase 10 (GalNAc-T10) GALNT5 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N- Cytoplasm enzyme acetylgalactosaminyltransferase 5 (GalNAc-T5) GBP3 guanylate binding protein 3 Cytoplasm enzyme GCM2 glial cells missing homolog 2 (Drosophila) Nucleus transcription regulator GDA guanine deaminase Cytoplasm enzyme GFAP glial fibrillary acidic protein Cytoplasm other GFRA1 GDNF family receptor alpha 1 Plasma Membrane transmembrane receptor GFRA2 GDNF family receptor alpha 2 Plasma Membrane transmembrane receptor GHRLOS ghrelin opposite strand/antisense RNA (non-protein unknown other coding) GIGYF1 GRB10 interacting GYF protein 1 unknown other GIPR gastric inhibitory polypeptide receptor Plasma Membrane G-protein coupled receptor GLI2 GLI family zinc finger 2 Nucleus transcription regulator GLP1R glucagon-like peptide 1 receptor Plasma Membrane G-protein coupled receptor GLRA1 glycine receptor, alpha 1 Plasma Membrane ion channel GNAL guanine nucleotide binding protein (G protein), alpha Cytoplasm enzyme activating activity polypeptide, olfactory type GNG8 guanine nucleotide binding protein (G protein), Plasma Membrane enzyme gamma 8 GPAM glycerol-3-phosphate acyltransferase, mitochondrial Cytoplasm enzyme GPC3 glypican 3 Plasma Membrane other GPR110 G protein-coupled receptor 110 Plasma Membrane G-protein coupled receptor GPR116 G protein-coupled receptor 116 Plasma Membrane G-protein coupled receptor GPR176 G protein-coupled receptor 176 Plasma Membrane G-protein coupled receptor GPR34 G protein-coupled receptor 34 Plasma Membrane G-protein coupled receptor GPR37 G protein-coupled receptor 37 (endothelin receptor Plasma Membrane G-protein type B-like) coupled receptor GPR4 G protein-coupled receptor 4 Plasma Membrane G-protein coupled receptor GPX6 glutathione peroxidase 6 (olfactory) Extracellular Space enzyme GPX8 glutathione peroxidase 8 (putative) unknown enzyme GRIA1 glutamate receptor, ionotropic, AMPA 1 Plasma Membrane ion channel GRIA2 glutamate receptor, ionotropic, AMPA 2 Plasma Membrane ion channel GRIA3 glutamate receptor, ionotropic, AMPA 3 Plasma Membrane ion channel GRIK2 glutamate receptor, ionotropic, kainate 2 Plasma Membrane ion channel GRIK3 glutamate receptor, ionotropic, kainate 3 Plasma Membrane ion channel GRM1 glutamate receptor, metabotropic 1 Plasma Membrane G-protein coupled receptor GRPR gastrin-releasing peptide receptor Plasma Membrane G-protein coupled receptor GSG1L GSG1-like unknown other GSN gelsolin Extracellular Space other GSTA1 glutathione S-transferase alpha 1 Cytoplasm enzyme GSTA5 glutathione S-transferase alpha 5 Cytoplasm enzyme GSTM3 glutathione S-transferase mu 3 (brain) Cytoplasm enzyme GUCY1A3 guanylate cyclase 1, soluble, alpha 3 Cytoplasm enzyme GUCY2F guanylate cyclase 2F, retinal Plasma Membrane kinase GVINP1 GTPase, very large interferon inducible pseudogene 1 Cytoplasm other HABP2 hyaluronan binding protein 2 Extracellular Space peptidase HAND1 heart and neural crest derivatives expressed 1 Nucleus transcription regulator HAND2 heart and neural crest derivatives expressed 2 Nucleus transcription regulator HAPLN1 hyaluronan and proteoglycan link protein 1 Extracellular Space other HCAR3 hydroxycarboxylic acid receptor 3 Plasma Membrane G-protein coupled receptor HCK hemopoietic cell kinase Cytoplasm kinase HDAC5 histone deacetylase 5 Nucleus transcription regulator HDAC9 histone deacetylase 9 Nucleus transcription regulator HESX1 HESX homeobox 1 Nucleus transcription regulator HGF hepatocyte growth factor (hepapoietin A; scatter Extracellular Space growth factor factor) HHIP hedgehog interacting protein Plasma Membrane other HHIPL1 HHIP-like 1 unknown other HIST1H2BN histone cluster 1, H2bn Nucleus other HIST1H4A (includes histone cluster 1, H4a Nucleus other others) HIVEP2 human immunodeficiency virus type I enhancer Nucleus transcription binding protein 2 regulator HMGCS2 3-hydroxy-3-methylglutaryl-CoA synthase 2 Cytoplasm enzyme (mitochondrial) HNF4G hepatocyte nuclear factor 4, gamma Nucleus transcription regulator HOXA2 homeobox A2 Nucleus transcription regulator HOXA9 homeobox A9 Nucleus transcription regulator HOXC8 homeobox C8 Nucleus transcription regulator HOXD10 homeobox D10 Nucleus transcription regulator HRASLS5 HRAS-like suppressor family, member 5 unknown other HSD17B13 hydroxysteroid (17-beta) dehydrogenase 13 Extracellular Space enzyme HTN3 histatin 3 Extracellular Space other HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G Plasma Membrane G-protein protein-coupled coupled receptor HTR3C 5-hydroxytryptamine (serotonin) receptor 3C, Plasma Membrane ion channel ionotropic HYDIN HYDIN, axonemal central pair apparatus protein unknown other IFFO1 intermediate filament family orphan 1 unknown other IFIT2 interferon-induced protein with tetratricopeptide Cytoplasm other repeats 2 IFNA16 interferon, alpha 16 Extracellular Space cytokine IGBP1 immunoglobulin (CD79A) binding protein 1 Cytoplasm phosphatase IGF2 insulin-like growth factor 2 (somatomedin A) Extracellular Space growth factor IKZF4 IKAROS family zinc finger 4 (Eos) Nucleus transcription regulator IL10 interleukin 10 Extracellular Space cytokine IL17B interleukin 17B Extracellular Space cytokine IL18 (includes interleukin 18 (interferon-gamma-inducing factor) Extracellular Space cytokine EG: 16173) IL1B interleukin 1, beta Extracellular Space cytokine IL1RAPL1 interleukin 1 receptor accessory protein-like 1 Plasma Membrane transmembrane receptor IL1RN interleukin 1 receptor antagonist Extracellular Space cytokine IL2 interleukin 2 Extracellular Space cytokine IL3 interleukin 3 (colony-stimulating factor, multiple) Extracellular Space other IL31 interleukin 31 unknown other IL6 interleukin 6 (interferon, beta 2) Extracellular Space cytokine IMPG1 interphotoreceptor matrix proteoglycan 1 Extracellular Space other INGX inhibitor of growth family, X-linked, pseudogene unknown other INPP5E inositol polyphosphate-5-phosphatase, 72 kDa Cytoplasm phosphatase INPP5K inositol polyphosphate-5-phosphatase K Cytoplasm phosphatase INSL5 insulin-like 5 Extracellular Space other IQCF1 IQ motif containing F1 unknown other IRS2 insulin receptor substrate 2 Cytoplasm enzyme IRX4 iroquois homeobox 4 Nucleus transcription regulator ISX intestine-specific homeobox unknown other ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen Plasma Membrane transmembrane CD61) receptor ITGBL1 integrin, beta-like 1 (with EGF-like repeat domains) unknown other JAK1 (includes Janus kinase 1 Cytoplasm kinase EG: 16451) JAKMIP3 Janus kinase and microtubule interacting protein 3 unknown other JARID2 jumonji, AT rich interactive domain 2 Nucleus transcription regulator JUN jun proto-oncogene Nucleus transcription regulator KANK2 KN motif and ankyrin repeat domains 2 Nucleus transcription regulator KCNA3 potassium voltage-gated channel, shaker-related Plasma Membrane ion channel subfamily, member 3 KCNA4 potassium voltage-gated channel, shaker-related Plasma Membrane ion channel subfamily, member 4 KCNA7 potassium voltage-gated channel, shaker-related Plasma Membrane ion channel subfamily, member 7 KCNAB1 potassium voltage-gated channel, shaker-related Plasma Membrane ion channel subfamily, beta member 1 KCNB2 potassium voltage-gated channel, Shab-related Plasma Membrane ion channel subfamily, member 2 KCNC1 potassium voltage-gated channel, Shaw-related Plasma Membrane ion channel subfamily, member 1 KCNC2 potassium voltage-gated channel, Shaw-related Plasma Membrane ion channel subfamily, member 2 KCND3 potassium voltage-gated channel, Shal-related Plasma Membrane ion channel subfamily, member 3 KCNG4 potassium voltage-gated channel, subfamily G, Plasma Membrane ion channel member 4 KCNH7 potassium voltage-gated channel, subfamily H (eag- Plasma Membrane ion channel related), member 7 KCNIP2 Kv channel interacting protein 2 Cytoplasm other KCNJ5 potassium inwardly-rectifying channel, subfamily J, Plasma Membrane ion channel member 5 KCNK10 potassium channel, subfamily K, member 10 Plasma Membrane ion channel KCNK17 potassium channel, subfamily K, member 17 Plasma Membrane ion channel KCNQ1 potassium voltage-gated channel, KQT-like Plasma Membrane ion channel subfamily, member 1 KCNQ1DN KCNQ1 downstream neighbor (non-protein coding) unknown other KCP (includes kielin/chordin-like protein Extracellular Space other EG: 296952) KCTD19 potassium channel tetramerisation domain containing unknown other 19 KCTD4 potassium channel tetramerisation domain containing 4 unknown ion channel KIAA0355 KIAA0355 unknown other KIAA0825 KIAA0825 unknown other KIAA1045 KIAA1045 unknown other KIAA1109 KIAA1109 unknown other KIAA1239 KIAA1239 unknown other KIAA1407 KIAA1407 unknown other KIAA1462 KIAA1462 unknown other KIAA1522 KIAA1522 unknown other KIAA1683 KIAA1683 Cytoplasm other KIF6 kinesin family member 6 Nucleus other KIRREL3 kin of IRRE like 3 (Drosophila) Extracellular Space other KL klotho Extracellular Space enzyme KLF12 Kruppel-like factor 12 Nucleus transcription regulator KLF2 Kruppel-like factor 2 (lung) Nucleus transcription regulator KLHDC9 kelch domain containing 9 unknown other KLHL24 kelch-like 24 (Drosophila) unknown other KLHL4 kelch-like 4 (Drosophila) Cytoplasm other KLRB1 killer cell lectin-like receptor subfamily B, member 1 Plasma Membrane transmembrane receptor KRT2 keratin 2 Cytoplasm other KRT6B keratin 6B Cytoplasm other KRT72 keratin 72 unknown other KRT75 keratin 75 Cytoplasm other KRT82 keratin 82 Cytoplasm other KRTAP1-1 keratin associated protein 1-1 unknown other KRTAP1-3 keratin associated protein 1-3 unknown other KRTAP15-1 keratin associated protein 15-1 unknown other KRTAP4-7 keratin associated protein 4-7 unknown other KRTAP9-2 keratin associated protein 9-2 unknown other LAIR2 leukocyte-associated immunoglobulin-like receptor 2 Plasma Membrane other LAMA1 laminin, alpha 1 Extracellular Space other LAYN layilin Plasma Membrane other LCE1E late cornified envelope 1E unknown other LECT1 leukocyte cell derived chemotaxin 1 Extracellular Space other LEF1 lymphoid enhancer-binding factor 1 Nucleus transcription regulator LEFTY1 left-right determination factor 1 Extracellular Space growth factor LEMD1 LEM domain containing 1 unknown other LEP leptin Extracellular Space growth factor LGALS13 lectin, galactoside-binding, soluble, 13 unknown enzyme LGALS2 lectin, galactoside-binding, soluble, 2 Cytoplasm other LGR5 leucine-rich repeat containing G protein-coupled Plasma Membrane G-protein receptor 5 coupled receptor LIFR leukemia inhibitory factor receptor alpha Plasma Membrane transmembrane receptor LILRB2 leukocyte immunoglobulin-like receptor, subfamily B Plasma Membrane other (with TM and ITIM domains), member 2 LINC00317 long intergenic non-protein coding RNA 317 unknown other LINC00477 long intergenic non-protein coding RNA 477 unknown other LIPF lipase, gastric Extracellular Space enzyme LOC100128098 uncharacterized LOC100128098 unknown other LOC100128108 uncharacterized LOC100128108 unknown other LOC100129406 uncharacterized LOC100129406 unknown other LOC100129476 uncharacterized LOC100129476 unknown other LOC100129775 uncharacterized LOC100129775 unknown other LOC100130278 uncharacterized LOC100130278 unknown other LOC100130776 uncharacterized LOC100130776 unknown other LOC100130815 uncharacterized LOC100130815 unknown other LOC100131176 uncharacterized LOC100131176 unknown other LOC100132116 uncharacterized LOC100132116 unknown other LOC100132363 uncharacterized LOC100132363 unknown other LOC100170939 glucuronidase, beta pseudogene unknown other LOC100190938 uncharacterized LOC100190938 unknown other LOC100190986 uncharacterized LOC100190986 unknown other LOC100288966/POTED POTE ankyrin domain family, member D Plasma Membrane other LOC120824/SPRYD5 SPRY domain containing 5 unknown other LOC283174 uncharacterized LOC283174 unknown other LOC283663 uncharacterized LOC283663 unknown other LOC283665 uncharacterized LOC283665 unknown other LOC284260 uncharacterized LOC284260 unknown other LOC284861 uncharacterized LOC284861 unknown other LOC286071 uncharacterized LOC286071 unknown other LOC286382 uncharacterized LOC286382 unknown other LOC339260 uncharacterized LOC339260 unknown other LOC389023 uncharacterized LOC389023 unknown other LOC389043 uncharacterized LOC389043 unknown other LOC390705 protein phosphatase 2, regulatory subunit B″, beta unknown other pseudogene LOC400620 uncharacterized LOC400620 unknown other LOC400655 uncharacterized LOC400655 unknown other LOC401317 uncharacterized LOC401317 unknown other LOC441601 septin 7 pseudogene unknown other LOC474358 uncharacterized BC042079 locus unknown other LOC644192 uncharacterized LOC644192 unknown other LOC646471 uncharacterized LOC646471 unknown other LOC646627 phospholipase inhibitor unknown other LOC647107 uncharacterized LOC647107 unknown other LOC647946 uncharacterized LOC647946 unknown other LOC728093/LOC729915 putative POM121-like protein 1 unknown other LOC728323 uncharacterized LOC728323 unknown other LOC729121 uncharacterized LOC729121 unknown other LOC729970 hCG2028352-like unknown other LOX (includes lysyl oxidase Extracellular Space enzyme EG: 16948) LOXL3 lysyl oxidase-like 3 Extracellular Space enzyme LOXL4 lysyl oxidase-like 4 Extracellular Space enzyme LPIN2 lipin 2 Nucleus phosphatase LRCH2 leucine-rich repeats and calponin homology (CH) unknown other domain containing 2 LRP1 (includes low density lipoprotein receptor-related protein 1 Plasma Membrane transmembrane EG: 16971) receptor LRP1B low density lipoprotein receptor-related protein 1B Plasma Membrane transmembrane receptor LRRC27 leucine rich repeat containing 27 unknown other LRRC37A3 (includes leucine rich repeat containing 37, member A3 unknown other others) LRRC48 leucine rich repeat containing 48 Cytoplasm other LRRC71 leucine rich repeat containing 71 unknown other LRRCC1 leucine rich repeat and coiled-coil domain containing 1 Nucleus transporter LTBP1 latent transforming growth factor beta binding protein 1 Extracellular Space other LUM lumican Extracellular Space other LYPD2 LY6/PLAUR domain containing 2 unknown other LYPD6 LY6/PLAUR domain containing 6 Extracellular Space other MACF1 microtubule-actin crosslinking factor 1 Cytoplasm enzyme MAEL maelstrom homolog (Drosophila) Cytoplasm other MAL mal, T-cell differentiation protein Plasma Membrane transporter MAPK4 mitogen-activated protein kinase 4 Cytoplasm kinase MAPT microtubule-associated protein tau Cytoplasm other MARK1 MAP/microtubule affinity-regulating kinase 1 Cytoplasm kinase MARVELD3 MARVEL domain containing 3 unknown other MAS1 MAS1 oncogene Plasma Membrane G-protein coupled receptor MBD3L2 (includes methyl-CpG binding domain protein 3-like 2 unknown other others) MBP myelin basic protein Extracellular Space other MCHR2 melanin-concentrating hormone receptor 2 Plasma Membrane G-protein coupled receptor MCTP1 multiple C2 domains, transmembrane 1 unknown other MECOM MDS1 and EVI1 complex locus Nucleus transcription regulator MEG3 maternally expressed 3 (non-protein coding) unknown other METTL21A methyltransferase like 21A unknown other METTL7A methyltransferase like 7A unknown other MFAP5 microfibrillar associated protein 5 Extracellular Space other MGC24103 uncharacterized MGC24103 unknown other MGC39545 uncharacterized LOC403312 unknown other MGC70870 C-terminal binding protein 2 pseudogene unknown other MGEA5 meningioma expressed antigen 5 (hyaluronidase) Cytoplasm enzyme MIA2 melanoma inhibitory activity 2 Extracellular Space other MIER1 mesoderm induction early response 1 homolog Nucleus other (Xenopus laevis) MIR7-3HG MIR7-3 host gene (non-protein coding) unknown other MIS18BP1 MIS18 binding protein 1 Nucleus other MLF1 myeloid leukemia factor 1 Nucleus other MLL myeloid/lymphoid or mixed-lineage leukemia Nucleus transcription (trithorax homolog, Drosophila) regulator MLLT4 myeloid/lymphoid or mixed-lineage leukemia Nucleus other (trithorax homolog, Drosophila); translocated to, 4 MME membrane metallo-endopeptidase Plasma Membrane peptidase MMP12 matrix metallopeptidase 12 (macrophage elastase) Extracellular Space peptidase MMP16 matrix metallopeptidase 16 (membrane-inserted) Extracellular Space peptidase MMP2 matrix metallopeptidase 2 (gelatinase A, 72 kDa Extracellular Space peptidase gelatinase, 72 kDa type IV collagenase) MMP8 matrix metallopeptidase 8 (neutrophil collagenase) Extracellular Space peptidase MMP9 matrix metallopeptidase 9 (gelatinase B, 92 kDa Extracellular Space peptidase gelatinase, 92 kDa type IV collagenase) MNT MAX binding protein Nucleus transcription regulator MORN5 MORN repeat containing 5 unknown other MOXD1 monooxygenase, DBH-like 1 Cytoplasm enzyme MPP4 membrane protein, palmitoylated 4 (MAGUK p55 Cytoplasm kinase subfamily member 4) MPPED2 metallophosphoesterase domain containing 2 unknown other MRO maestro Nucleus other MSMB microseminoprotein, beta- Extracellular Space other MTHFR methylenetetrahydrofolate reductase (NAD(P)H) Cytoplasm enzyme MTL5 metallothionein-like 5, testis-specific (tesmin) Cytoplasm other MTMR7 myotubularin related protein 7 Cytoplasm phosphatase MUC17 mucin 17, cell surface associated Plasma Membrane other MXI1 MAX interactor 1 Nucleus transcription regulator MYCL1 v-myc myelocytomatosis viral oncogene homolog 1, Nucleus transcription lung carcinoma derived (avian) regulator MYF6 myogenic factor 6 (herculin) Nucleus transcription regulator MYO16 myosin XVI Cytoplasm other MYO3B myosin IIIB unknown kinase MYOM1 myomesin 1, 185 kDa Cytoplasm other MYOZ1 myozenin 1 Cytoplasm other MYPN myopalladin Cytoplasm other N4BP2L1 NEDD4 binding protein 2-like 1 unknown other NAG20 NAG20 unknown other NAV1 neuron navigator 1 Cytoplasm enzyme NAV2 neuron navigator 2 Nucleus other NBR1 neighbor of BRCA1 gene 1 Cytoplasm other NDRG2 NDRG family member 2 Cytoplasm other NECAB2 N-terminal EF-hand calcium binding protein 2 Cytoplasm other NEGR1 neuronal growth regulator 1 Extracellular Space other NEUROD4 neuronal differentiation 4 Nucleus other NEXN-AS1 NEXN antisense RNA 1 (non-protein coding) unknown other NFIB nuclear factor I/B Nucleus transcription regulator NIPBL Nipped-B homolog (Drosophila) Nucleus transcription regulator NKX3-2 NK3 homeobox 2 Nucleus transcription regulator NLRP13 NLR family, pyrin domain containing 13 unknown other NMNAT2 nicotinamide nucleotide adenylyltransferase 2 Cytoplasm enzyme NMU neuromedin U Extracellular Space other NOTCH2NL notch 2 N-terminal like unknown other NOX1 NADPH oxidase 1 Cytoplasm ion channel NPTX1 neuronal pentraxin I Extracellular Space other NR2F2 nuclear receptor subfamily 2, group F, member 2 Nucleus ligand- dependent nuclear receptor NR4A1 nuclear receptor subfamily 4, group A, member 1 Nucleus ligand- dependent nuclear receptor NR4A2 nuclear receptor subfamily 4, group A, member 2 Nucleus ligand- dependent nuclear receptor NRG2 neuregulin 2 Extracellular Space growth factor NRIP2 nuclear receptor interacting protein 2 Nucleus transcription regulator NRXN3 neurexin 3 Plasma Membrane transporter NSUN7 NOP2/Sun domain family, member 7 unknown other NTN4 netrin 4 Extracellular Space other NTSR1 neurotensin receptor 1 (high affinity) Plasma Membrane G-protein coupled receptor NUDT9P1 nudix (nucleoside diphosphate linked moiety X)-type unknown other motif 9 pseudogene 1 NUP210P1 nucleoporin 210 kDa pseudogene 1 unknown other NYAP1 neuronal tyrosine-phosphorylated phosphoinositide- unknown other 3-kinase adaptor 1 OCA2 (includes oculocutaneous albinism II Plasma Membrane transporter EG: 18431) ODF1 outer dense fiber of sperm tails 1 Cytoplasm other OGN osteoglycin Extracellular Space growth factor OIT3 oncoprotein induced transcript 3 Nucleus other OLFML2A olfactomedin-like 2A Extracellular Space other OLIG2 oligodendrocyte lineage transcription factor 2 Nucleus transcription regulator OPRM1 opioid receptor, mu 1 Plasma Membrane G-protein coupled receptor OR10J1 olfactory receptor, family 10, subfamily J, member 1 Plasma Membrane G-protein coupled receptor OR10T2 olfactory receptor, family 10, subfamily T, member 2 Plasma Membrane other OR1E1 olfactory receptor, family 1, subfamily E, member 1 Plasma Membrane G-protein coupled receptor OR2C3 olfactory receptor, family 2, subfamily C, member 3 Plasma Membrane other OR2L13 olfactory receptor, family 2, subfamily L, member 13 Plasma Membrane G-protein coupled receptor OR2S2 olfactory receptor, family 2, subfamily S, member 2 Plasma Membrane G-protein coupled receptor OR2V2 olfactory receptor, family 2, subfamily V, member 2 Plasma Membrane G-protein coupled receptor OR4N4 olfactory receptor, family 4, subfamily N, member 4 Plasma Membrane G-protein coupled receptor OR51E1 olfactory receptor, family 51, subfamily E, member 1 Plasma Membrane G-protein coupled receptor OR51E2 olfactory receptor, family 51, subfamily E, member 2 Plasma Membrane G-protein coupled receptor OR51Q1 olfactory receptor, family 51, subfamily Q, member 1 Plasma Membrane G-protein coupled receptor OR52B2 olfactory receptor, family 52, subfamily B, member 2 Plasma Membrane G-protein coupled receptor OR5AK2 olfactory receptor, family 5, subfamily AK, member 2 Plasma Membrane G-protein coupled receptor OSBPL2 oxysterol binding protein-like 2 Cytoplasm other OSTalpha organic solute transporter alpha Plasma Membrane transporter OTX1 orthodenticle homeobox 1 Nucleus transcription regulator OVOL1 ovo-like 1(Drosophila) Nucleus transcription regulator P2RY13 purinergic receptor P2Y, G-protein coupled, 13 Plasma Membrane G-protein coupled receptor P2RY14 purinergic receptor P2Y, G-protein coupled, 14 Plasma Membrane G-protein coupled receptor PABPC5 poly(A) binding protein, cytoplasmic 5 Cytoplasm other PAOX polyamine oxidase (exo-N4-amino) Cytoplasm enzyme PARVA parvin, alpha Cytoplasm other PASD1 PAS domain containing 1 Nucleus other PAX3 paired box 3 Nucleus transcription regulator PCDH11X/PCDH11Y protocadherin 11 Y-linked Plasma Membrane other PCDH18 protocadherin 18 Extracellular Space other PCDH7 protocadherin 7 Plasma Membrane other PCDHB10 protocadherin beta 10 Plasma Membrane other PCDHB5 protocadherin beta 5 Plasma Membrane other PCDHGA9 protocadherin gamma subfamily A, 9 unknown other PCDHGB8P protocadherin gamma subfamily B, 8 pseudogene unknown other PCMTD2 protein-L-isoaspartate (D-aspartate) O- Cytoplasm enzyme methyltransferase domain containing 2 PCNXL2 pecanex-like 2 (Drosophila) unknown other PCSK2 proprotein convertase subtilisin/kexin type 2 Extracellular Space peptidase PDC phosducin Cytoplasm other PDCD4 programmed cell death 4 (neoplastic transformation Nucleus other inhibitor) PDE1A phosphodiesterase 1A, calmodulin-dependent Cytoplasm enzyme PDE4C phosphodiesterase 4C, cAMP-specific Cytoplasm enzyme PDE4DIP phosphodiesterase 4D interacting protein Cytoplasm enzyme PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha Plasma Membrane enzyme PDE8B phosphodiesterase 8B Cytoplasm enzyme PDK4 pyruvate dehydrogenase kinase, isozyme 4 Cytoplasm kinase PDLIM3 PDZ and LIM domain 3 Cytoplasm other PDZD9 PDZ domain containing 9 unknown other PDZRN4 PDZ domain containing ring finger 4 unknown other PES1 pescadillo ribosomal biogenesis factor 1 Nucleus other PEX5L peroxisomal biogenesis factor 5-like Cytoplasm ion channel PHACTR1 phosphatase and actin regulator 1 Cytoplasm other PHF12 PHD finger protein 12 Nucleus transcription regulator PHLDA3 pleckstrin homology-like domain, family A, member 3 Plasma Membrane other PHLDB2 pleckstrin homology-like domain, family B, member 2 Cytoplasm other PHYHD1 phytanoyl-CoA dioxygenase domain containing 1 unknown other PHYHIPL phytanoyl-CoA 2-hydroxylase interacting protein-like Cytoplasm other PIM1 pim-1 oncogene Cytoplasm kinase PIP prolactin-induced protein Extracellular Space other PITPNM2 phosphatidylinositol transfer protein, membrane- Cytoplasm enzyme associated 2 PKD1L1 polycystic kidney disease 1 like 1 Extracellular Space other PKHD1 polycystic kidney and hepatic disease 1 (autosomal Plasma Membrane other recessive) PKP1 plakophilin 1 (ectodermal dysplasia/skin fragility Plasma Membrane other syndrome) PLA2R1 phospholipase A2 receptor 1, 180 kDa Plasma Membrane transmembrane receptor PLAT plasminogen activator, tissue Extracellular Space peptidase PLB1 (includes phospholipase B1 Cytoplasm enzyme EG: 151056) PLCD4 phospholipase C, delta 4 Cytoplasm enzyme PLCH1 phospholipase C, eta 1 Cytoplasm enzyme PLCZ1 phospholipase C, zeta 1 unknown enzyme PLD1 phospholipase D1, phosphatidylcholine-specific Cytoplasm enzyme PLD3 phospholipase D family, member 3 Cytoplasm enzyme PLEKHA6 pleckstrin homology domain containing, family A unknown other member 6 PLEKHH2 pleckstrin homology domain containing, family H Cytoplasm other (with MyTH4 domain) member 2 PLGLB1/PLGLB2 plasminogen-like B2 Extracellular Space peptidase PLN phospholamban Cytoplasm other PLSCR2 phospholipid scramblase 2 unknown other PLSCR4 phospholipid scramblase 4 Plasma Membrane enzyme PM20D1 peptidase M20 domain containing 1 unknown peptidase PMCH pro-melanin-concentrating hormone Extracellular Space other PMCHL1 pro-melanin-concentrating hormone-like 1, Extracellular Space other pseudogene PNLIP pancreatic lipase Extracellular Space enzyme PNPLA1 patatin-like phospholipase domain containing 1 unknown enzyme PNRC1 proline-rich nuclear receptor coactivator 1 Nucleus other POLK polymerase (DNA directed) kappa Nucleus enzyme POLR2M polymerase (RNA) II (DNA directed) polypeptide M Nucleus other PON3 paraoxonase 3 Extracellular Space enzyme POTEE/POTEF POTE ankyrin domain family, member F unknown other POU4F2 POU class 4 homeobox 2 Nucleus transcription regulator PPAPDC1A phosphatidic acid phosphatase type 2 domain unknown phosphatase containing 1A PPIC peptidylprolyl isomerase C (cyclophilin C) Cytoplasm enzyme PRICKLE2 prickle homolog 2 (Drosophila) Nucleus other PRKAA2 protein kinase, AMP-activated, alpha 2 catalytic Cytoplasm kinase subunit PRKG1 protein kinase, cGMP-dependent, type I Cytoplasm kinase PRODH2 proline dehydrogenase (oxidase) 2 Cytoplasm enzyme PRR16 proline rich 16 unknown other PRSS23 protease, serine, 23 Extracellular Space peptidase PSORS1C1 psoriasis susceptibility 1 candidate 1 unknown other PTCH1 patched 1 Plasma Membrane transmembrane receptor PTGER3 prostaglandin E receptor 3 (subtype EP3) Plasma Membrane G-protein coupled receptor PTGS2 prostaglandin-endoperoxide synthase 2 Cytoplasm enzyme (prostaglandin G/H synthase and cyclooxygenase) PTPRC protein tyrosine phosphatase, receptor type, C Plasma Membrane phosphatase PTPRZ1 protein tyrosine phosphatase, receptor-type, Z Plasma Membrane phosphatase polypeptide 1 PYCR1 pyrroline-5-carboxylate reductase 1 Cytoplasm enzyme PZP pregnancy-zone protein Extracellular Space other RAB37 RAB37, member RAS oncogene family Cytoplasm enzyme RAB39A RAB39A, member RAS oncogene family Cytoplasm enzyme RAB3C (includes RAB3C, member RAS oncogene family Cytoplasm enzyme EG: 115827) RAET1E retinoic acid early transcript 1E Plasma Membrane other RAG1 recombination activating gene 1 Nucleus enzyme RAMP1 receptor (G protein-coupled) activity modifying Plasma Membrane transporter protein 1 RAVER2 ribonucleoprotein, PTB-binding 2 Nucleus other RBMY1A1 (includes RNA binding motif protein, Y-linked, family 1, Nucleus other others) member A1 RBPMS2 RNA binding protein with multiple splicing 2 unknown other RERGL RERG/RAS-like unknown other REST RE1-silencing transcription factor Nucleus transcription regulator RET ret proto-oncogene Plasma Membrane kinase REXO1L1 (includes REX1, RNA exonuclease 1 homolog (S. cerevisiae)- unknown enzyme others) like 1 RGNEF 190 kDa guanine nucleotide exchange factor Cytoplasm other RHO rhodopsin Plasma Membrane G-protein coupled receptor RHOT1 ras homolog family member T1 Cytoplasm enzyme RIMBP3 (includes RIMS binding protein 3 Nucleus other others) RIMS2 regulating synaptic membrane exocytosis 2 unknown other RIN2 Ras and Rab interactor 2 Cytoplasm other RIT2 Ras-like without CAAX 2 Plasma Membrane enzyme RMI2 RMI2, RecQ mediated genome instability 2, homolog unknown other (S. cerevisiae) RND3 Rho family GTPase 3 Cytoplasm enzyme RNF125 ring finger protein 125, E3 ubiquitin protein ligase unknown other RNF128 ring finger protein 128, E3 ubiquitin protein ligase Cytoplasm enzyme RNF133 ring finger protein 133 Cytoplasm other RNF175 ring finger protein 175 unknown other RNF8 ring finger protein 8, E3 ubiquitin protein ligase Nucleus enzyme RORB RAR-related orphan receptor B Nucleus ligand- dependent nuclear receptor RPL32P3 ribosomal protein L32 pseudogene 3 unknown other RPS6KB1 ribosomal protein S6 kinase, 70 kDa, polypeptide 1 Cytoplasm kinase RRAD Ras-related associated with diabetes Cytoplasm enzyme RUFY2 RUN and FYVE domain containing 2 Nucleus other RUNX1T1 runt-related transcription factor 1; translocated to, 1 Nucleus transcription (cyclin D-related) regulator RUNX2 runt-related transcription factor 2 Nucleus transcription regulator SALL3 sal-like 3 (Drosophila) Nucleus other SCARNA17 small Cajal body-specific RNA 17 unknown other SCGN secretagogin, EF-hand calcium binding protein Cytoplasm other SCN3B sodium channel, voltage-gated, type III, beta subunit Plasma Membrane ion channel SCN8A sodium channel, voltage gated, type VIII, alpha Plasma Membrane ion channel subunit SEMA4C sema domain, immunoglobulin domain (Ig), Plasma Membrane other transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C SEMA5A sema domain, seven thrombospondin repeats (type 1 Plasma Membrane transmembrane and type 1-like), transmembrane domain (TM) and receptor short cytoplasmic domain, (semaphorin) 5A SEMA6A sema domain, transmembrane domain (TM), and Plasma Membrane other cytoplasmic domain, (semaphorin) 6A SEMG2 semenogelin II Extracellular Space other SERPINA10 serpin peptidase inhibitor, clade A (alpha-1 Extracellular Space other antiproteinase, antitrypsin), member 10 SERPINB3 serpin peptidase inhibitor, clade B (ovalbumin), Extracellular Space other member 3 SERPINB4 serpin peptidase inhibitor, clade B (ovalbumin), Cytoplasm other member 4 SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), Extracellular Space other member 1 SERPINE1 serpin peptidase inhibitor, clade E (nexin, Extracellular Space other plasminogen activator inhibitor type 1), member 1 SERTAD4 SERTA domain containing 4 unknown other SGCD sarcoglycan, delta (35 kDa dystrophin-associated Cytoplasm other glycoprotein) SGCZ sarcoglycan, zeta Plasma Membrane other SGTA small glutamine-rich tetratricopeptide repeat (TPR)- Cytoplasm other containing, alpha SH3PXD2A SH3 and PX domains 2A Cytoplasm other SHANK3 SH3 and multiple ankyrin repeat domains 3 Cytoplasm transcription regulator SHROOM2 shroom family member 2 Plasma Membrane ion channel SHROOM4 shroom family member 4 Plasma Membrane other SIGLEC1 sialic acid binding Ig-like lectin 1, sialoadhesin Plasma Membrane other SIM2 single-minded homolog 2 (Drosophila) Nucleus transcription regulator SLC13A1 solute carrier family 13 (sodium/sulfate symporters), Plasma Membrane transporter member 1 SLC15A1 solute carrier family 15 (oligopeptide transporter), Plasma Membrane transporter member 1 SLC16A5 solute carrier family 16, member 5 (monocarboxylic Plasma Membrane transporter acid transporter 6) SLC18A1 solute carrier family 18 (vesicular monoamine), Plasma Membrane transporter member 1 SLC18A3 solute carrier family 18 (vesicular acetylcholine), Plasma Membrane transporter member 3 SLC19A3 solute carrier family 19, member 3 Plasma Membrane transporter SLC22A18 solute carrier family 22, member 18 Plasma Membrane transporter SLC22A9 solute carrier family 22 (organic anion transporter), Plasma Membrane transporter member 9 SLC25A27 solute carrier family 25, member 27 Cytoplasm transporter SLC25A36 solute carrier family 25, member 36 Cytoplasm transporter SLC35F3 solute carrier family 35, member F3 unknown other SLC38A3 solute carrier family 38, member 3 Plasma Membrane transporter SLC46A2 solute carrier family 46, member 2 Plasma Membrane transporter SLC4A2 solute carrier family 4, anion exchanger, member 2 Plasma Membrane transporter (erythrocyte membrane protein band 3-like 1) SLC6A1 solute carrier family 6 (neurotransmitter transporter, Plasma Membrane transporter GABA), member 1 SLC6A11 solute carrier family 6 (neurotransmitter transporter, Plasma Membrane transporter GABA), member 11 SLC6A15 solute carrier family 6 (neutral amino acid Plasma Membrane transporter transporter), member 15 SLC6A19 solute carrier family 6 (neutral amino acid Plasma Membrane transporter transporter), member 19 SLC9B1 solute carrier family 9, subfamily B (NHA1, cation Plasma Membrane other proton antiporter 1), member 1 SLCO1A2 solute carrier organic anion transporter family, Plasma Membrane transporter member 1A2 SLFN5 schlafen family member 5 Nucleus enzyme SLITRK1 SLIT and NTRK-like family, member 1 unknown other SLITRK5 SLIT and NTRK-like family, member 5 unknown other SMA4 glucuronidase, beta pseudogene unknown other SMAD3 SMAD family member 3 Nucleus transcription regulator SMG1 smg-1 homolog, phosphatidylinositol 3-kinase-related Cytoplasm kinase kinase (C. elegans) SMOC1 SPARC related modular calcium binding 1 Extracellular Space other SNTB1 syntrophin, beta 1 (dystrophin-associated protein A1, Plasma Membrane other 59 kDa, basic component 1) SOCS2 suppressor of cytokine signaling 2 Cytoplasm other SORBS2 sorbin and SH3 domain containing 2 Plasma Membrane other SOX11 SRY (sex determining region Y)-box 11 Nucleus transcription regulator SOX21 SRY (sex determining region Y)-box 21 Nucleus transcription regulator SOX7 SRY (sex determining region Y)-box 7 Nucleus transcription regulator SP100 SP100 nuclear antigen Nucleus transcription regulator SPATA17 spermatogenesis associated 17 unknown other SPDYA speedy homolog A (Xenopus laevis) Nucleus other SPINLW1 serine peptidase inhibitor-like, with Kunitz and WAP Extracellular Space other domains 1 (eppin) SPOCK1 sparc/osteonectin, cwcv and kazal-like domains Extracellular Space other proteoglycan (testican) 1 SPP1 (includes secreted phosphoprotein 1 Extracellular Space cytokine EG: 20750) SPRED2 sprouty-related, EVH1 domain containing 2 Extracellular Space cytokine SPSB3 splA/ryanodine receptor domain and SOCS box unknown other containing 3 SPTB spectrin, beta, erythrocytic Plasma Membrane other SSBP1 single-stranded DNA binding protein 1 Cytoplasm other SSPO SCO-spondin homolog (Bos taurus) Cytoplasm other SSTR1 somatostatin receptor 1 Plasma Membrane G-protein coupled receptor SSX4/SSX4B synovial sarcoma, X breakpoint 4 Nucleus other SSX8 synovial sarcoma, X breakpoint 8 unknown other ST3GAL6 ST3 beta-galactoside alpha-2,3-sialyltransferase 6 Cytoplasm enzyme ST6GAL2 ST6 beta-galactosamide alpha-2,6-sialyltranferase 2 Cytoplasm enzyme ST6GALNAC2 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl- Cytoplasm enzyme 1,3)-N-acetylgalactosaminide alpha-2,6- sialyltransferase 2 STAG3L1 stromal antigen 3-like 1 unknown other STARD13 StAR-related lipid transfer (START) domain Cytoplasm other containing 13 STK31 serine/threonine kinase 31 Cytoplasm kinase STK32B serine/threonine kinase 32B unknown kinase STMN1 stathmin 1 Cytoplasm other STMN3 stathmin-like 3 Nucleus other STON1-GTF2A1L STON1-GTF2A1L readthrough Nucleus transcription regulator STRA8 stimulated by retinoic acid gene 8 homolog (mouse) unknown other STS steroid sulfatase (microsomal), isozyme S Cytoplasm enzyme STX1B syntaxin 1B Plasma Membrane ion channel SYCE2 synaptonemal complex central element protein 2 Nucleus other SYCP3 synaptonemal complex protein 3 Nucleus other SYNE2 spectrin repeat containing, nuclear envelope 2 Nucleus other SYNPO2 synaptopodin 2 Cytoplasm other SYT14 synaptotagmin XIV unknown transporter TAC1 tachykinin, precursor 1 Extracellular Space other TACSTD2 tumor-associated calcium signal transducer 2 Plasma Membrane other tAKR aldo-keto reductase, truncated unknown enzyme TAOK1 TAO kinase 1 Cytoplasm kinase TAS2R42 taste receptor, type 2, member 42 unknown other TBX4 T-box 4 Nucleus transcription regulator TCEA3 transcription elongation factor A (SII), 3 Nucleus transcription regulator TCF12 transcription factor 12 Nucleus transcription regulator TCL1B T-cell leukemia/lymphoma 1B unknown other TCTEX1D1 Tctex1 domain containing 1 unknown other TDH L-threonine dehydrogenase Cytoplasm enzyme TEDDM1 transmembrane epididymal protein 1 unknown other TFAP2A transcription factor AP-2 alpha (activating enhancer Nucleus transcription binding protein 2 alpha) regulator TFAP2D transcription factor AP-2 delta (activating enhancer Nucleus transcription binding protein 2 delta) regulator TGFB3 transforming growth factor, beta 3 Extracellular Space growth factor TGM4 transglutaminase 4 (prostate) Extracellular Space enzyme THBS1 thrombospondin 1 Extracellular Space other THPO thrombopoietin Extracellular Space cytokine THRA (includes thyroid hormone receptor, alpha Nucleus ligand- EG: 21833) dependent nuclear receptor THSD7B thrombospondin, type I, domain containing 7B unknown other TIMM17B translocase of inner mitochondrial membrane 17 Cytoplasm transporter homolog B (yeast) TIMP2 (includes TIMP metallopeptidase inhibitor 2 Extracellular Space other EG: 21858) TINAG tubulointerstitial nephritis antigen Extracellular Space peptidase TLL1 tolloid-like 1 Extracellular Space peptidase TLR4 toll-like receptor 4 Plasma Membrane transmembrane receptor TLX1 T-cell leukemia homeobox 1 Nucleus transcription regulator TM4SF18 transmembrane 4 L six family member 18 unknown other TM4SF4 transmembrane 4 L six family member 4 Plasma Membrane other TMC3 transmembrane channel-like 3 unknown other TMEM192 transmembrane protein 192 unknown other TMEM37 transmembrane protein 37 Plasma Membrane ion channel TMEM45B transmembrane protein 45B Extracellular Space other TMEM47 transmembrane protein 47 Plasma Membrane other TMEM56 transmembrane protein 56 unknown other TMPRSS11A transmembrane protease, serine 11A unknown peptidase TNFAIP6 tumor necrosis factor, alpha-induced protein 6 Extracellular Space other TNFRSF10C tumor necrosis factor receptor superfamily, member Plasma Membrane transmembrane 10c, decoy without an intracellular domain receptor TNFRSF19 tumor necrosis factor receptor superfamily, member Plasma Membrane transmembrane 19 receptor TP73 tumor protein p73 Nucleus transcription regulator TPSD1 tryptase delta 1 Extracellular Space peptidase TRAM2 translocation associated membrane protein 2 unknown other TRIB1 tribbles homolog 1 (Drosophila) Cytoplasm kinase TRIM22 tripartite motif containing 22 Cytoplasm transcription regulator TRIM34 tripartite motif containing 34 Cytoplasm other TRIM49 tripartite motif containing 49 unknown other TRIM6 tripartite motif containing 6 Cytoplasm other TRIM72 tripartite motif containing 72 Cytoplasm other TRIML1 tripartite motif family-like 1 unknown other TRIML2 tripartite motif family-like 2 unknown other TRPM1 transient receptor potential cation channel, subfamily Plasma Membrane ion channel M, member 1 TRPM6 transient receptor potential cation channel, subfamily Plasma Membrane kinase M, member 6 TRPV1 transient receptor potential cation channel, subfamily Plasma Membrane ion channel V, member 1 TSPAN11 tetraspanin 11 unknown other TSPAN12 tetraspanin 12 Plasma Membrane transmembrane receptor TSPAN8 tetraspanin 8 Plasma Membrane other TTC18 tetratricopeptide repeat domain 18 unknown other TTC23L tetratricopeptide repeat domain 23-like unknown other TTLL10 tubulin tyrosine ligase-like family, member 10 Extracellular Space other TTN (includes titin Cytoplasm kinase EG: 22138) TTPA tocopherol (alpha) transfer protein Cytoplasm transporter TTTY2 testis-specific transcript, Y-linked 2 (non-protein Nucleus other coding) TTTY8 testis-specific transcript, Y-linked 8 (non-protein unknown other coding) TUSC5 tumor suppressor candidate 5 unknown other TXNRD2 thioredoxin reductase 2 Cytoplasm enzyme UACA uveal autoantigen with coiled-coil domains and Cytoplasm other ankyrin repeats UBE2M ubiquitin-conjugating enzyme E2M Cytoplasm enzyme UBE2R2 ubiquitin-conjugating enzyme E2R 2 unknown enzyme UBN2 ubinuclein 2 Nucleus other UCA1 urothelial cancer associated 1 (non-protein coding) unknown other UCP1 uncoupling protein 1 (mitochondrial, proton carrier) Cytoplasm transporter UGT3A1 UDP glycosyltransferase 3 family, polypeptide A1 unknown enzyme ULK2 unc-51-like kinase 2 (C. elegans) Cytoplasm kinase UNC80 unc-80 homolog (C. elegans) unknown other USP11 ubiquitin specific peptidase 11 Nucleus peptidase USP38 ubiquitin specific peptidase 38 unknown peptidase UTS2 urotensin 2 Extracellular Space other UTS2D urotensin 2 domain containing Extracellular Space other VEZF1 vascular endothelial zinc finger 1 Nucleus transcription regulator VN1R4 vomeronasal 1 receptor 4 Plasma Membrane G-protein coupled receptor VPS54 (includes vacuolar protein sorting 54 homolog (S. cerevisiae) unknown other EG: 245944) VSNL1 visinin-like 1 Cytoplasm other VSTM4 V-set and transmembrane domain containing 4 unknown other VWA1 von Willebrand factor A domain containing 1 Extracellular Space other VWA3B von Willebrand factor A domain containing 3B unknown other WASF2 WAS protein family, member 2 Cytoplasm other WDFY3-AS2 WDFY3 antisense RNA 2 (non-protein coding) unknown other WDR17 WD repeat domain 17 unknown other WDR45 WD repeat domain 45 unknown other WDR49 WD repeat domain 49 unknown other WDR65 WD repeat domain 65 unknown other WDR72 WD repeat domain 72 unknown other WDR96 WD repeat domain 96 unknown other WFDC11 WAP four-disulfide core domain 11 Extracellular Space other WFDC5 WAP four-disulfide core domain 5 Extracellular Space other WFDC6 WAP four-disulfide core domain 6 Extracellular Space other WFDC9 WAP four-disulfide core domain 9 Extracellular Space other WLS wntless homolog (Drosophila) Cytoplasm other WNT8B wingless-type MMTV integration site family, member Extracellular Space other 8B WWP2 WW domain containing E3 ubiquitin protein ligase 2 Cytoplasm enzyme XIRP2 xin actin-binding repeat containing 2 unknown other XRN1 5′-3′ exoribonuclease 1 Cytoplasm enzyme XYLB xylulokinase homolog (H. influenzae) unknown kinase YPEL1 yippee-like 1 (Drosophila) Nucleus enzyme YPEL2 yippee-like 2 (Drosophila) Nucleus other YPEL5 yippee-like 5 (Drosophila) unknown other ZADH2 zinc binding alcohol dehydrogenase domain Cytoplasm enzyme containing 2 ZBTB10 zinc finger and BTB domain containing 10 Nucleus other ZBTB20 zinc finger and BTB domain containing 20 Nucleus other ZC3H6 zinc finger CCCH-type containing 6 unknown other ZCCHC12 zinc finger, CCHC domain containing 12 unknown other ZDHHC15 zinc finger, DHHC-type containing 15 unknown enzyme ZFYVE16 zinc finger, FYVE domain containing 16 Nucleus transporter ZIC4 Zic family member 4 Nucleus other ZMAT1 zinc finger, matrin-type 1 Nucleus other ZNF292 zinc finger protein 292 Nucleus transcription regulator ZNF385B zinc finger protein 385B Nucleus other ZNF445 zinc finger protein 445 Nucleus transcription regulator ZNF45 zinc finger protein 45 Nucleus transcription regulator ZNF471 zinc finger protein 471 Nucleus other ZNF572 zinc finger protein 572 Nucleus other ZNF695 zinc finger protein 695 Nucleus other ZNF704 zinc finger protein 704 unknown other ZNF711 zinc finger protein 711 Nucleus other ZNF804A zinc finger protein 804A unknown other ZNF81 zinc finger protein 81 Nucleus transcription regulator ZSCAN4 zinc finger and SCAN domain containing 4 Nucleus transcription regulator

TABLE 2 Rapamycin-sensitive genes differentially regulated in brain of Alzheimer's disease patients with mild disease (112 known genes) Fold Symbol Entrez Gene Name Location Type(s) Change ABTB1 ankyrin repeat and BTB (POZ) domain containing 1 Cytoplasm translation regulator 1.057 ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 Extracellular Space peptidase 1.083 ADAMTSL5 ADAMTS-like 5 Extracellular Space other 1.088 AHNAK2 AHNAK nucleoprotein 2 unknown other 1.056 B4GALT6 UDP-Gal: betaGlcNAc beta 1,4-galactosyltransferase, Cytoplasm enzyme 1.022 polypeptide 6 BARX2 BARX homeobox 2 Nucleus transcription regulator 1.077 BMP7 bone morphogenetic protein 7 Extracellular Space growth factor 1.035 BTNL9 butyrophilin-like 9 unknown other 1.056 C17orf99 chromosome 17 open reading frame 99 unknown other 1.032 C1orf127 chromosome 1 open reading frame 127 unknown other 1.074 CACNA1D calcium channel, voltage-dependent, L type, alpha 1D Plasma Membrane ion channel 1.063 subunit CARD14 caspase recruitment domain family, member 14 Cytoplasm other 1.034 CC2D2A coiled-coil and C2 domain containing 2A unknown other 1.102 CCL1 chemokine (C-C motif) ligand 1 Extracellular Space cytokine 1.066 CCL11 chemokine (C-C motif) ligand 11 Extracellular Space cytokine 1.048 CCL2 chemokine (C-C motif) ligand 2 Extracellular Space cytokine 1.061 CCR1 chemokine (C-C motif) receptor 1 Plasma Membrane G-protein coupled 1.034 receptor CD69 CD69 molecule Plasma Membrane transmembrane 1.028 receptor CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4) Nucleus transcription regulator 1.056 CEACAM1 carcinoembryonic antigen-related cell adhesion molecule 1 Plasma Membrane transmembrane 1.079 (includes others) (biliary glycoprotein) receptor CEP68 centrosomal protein 68 kDa Cytoplasm other 1.036 COL1A2 collagen, type I, alpha 2 Extracellular Space other 1.043 CPXM2 carboxypeptidase X (M14 family), member 2 Extracellular Space peptidase 1.026 CREB3L4 cAMP responsive element binding protein 3-like 4 Nucleus transcription regulator 1.064 CRP C-reactive protein, pentraxin-related Extracellular Space other 1.104 CTDSP1 CTD (carboxy-terminal domain, RNA polymerase II, Nucleus phosphatase 1.098 polypeptide A) small phosphatase 1 DCAF12L1 DDB1 and CUL4 associated factor 12-like 1 unknown other 1.030 DCD dermcidin Extracellular Space other 1.159 DRP2 dystrophin related protein 2 Plasma Membrane other 1.043 EBF2 early B-cell factor 2 Nucleus other 1.028 ENTPD8 ectonucleoside triphosphate diphosphohydrolase 8 unknown enzyme 1.071 FAM43B family with sequence similarity 43, member B unknown other 1.061 FAM64A family with sequence similarity 64, member A Nucleus other 1.214 FCGBP Fc fragment of IgG binding protein Extracellular Space other 1.057 FGF11 fibroblast growth factor 11 Extracellular Space growth factor 1.169 FJX1 four jointed box 1 (Drosophila) Extracellular Space other 1.123 FLJ35946 uncharacterized protein FLJ35946 unknown other 1.148 FN3K fructosamine 3 kinase Cytoplasm kinase 1.258 GLI2 GLI family zinc finger 2 Nucleus transcription regulator 1.032 GLP1R glucagon-like peptide 1 receptor Plasma Membrane G-protein coupled 1.031 receptor GLRA1 glycine receptor, alpha 1 Plasma Membrane ion channel 1.041 GPR176 G protein-coupled receptor 176 Plasma Membrane G-protein coupled 1.092 receptor HCAR3 hydroxycarboxylic acid receptor 3 Plasma Membrane G-protein coupled 1.041 receptor HDAC5 histone deacetylase 5 Nucleus transcription regulator 1.112 HHIPL1 HHIP-like 1 unknown other 1.057 HMGCS2 3-hydroxy-3-methylglutaryl-CoA synthase 2 (mitochondrial) Cytoplasm enzyme 1.044 HOXD10 homeobox D10 Nucleus transcription regulator 1.024 HYDIN HYDIN, axonemal central pair apparatus protein unknown other 1.077 IL6 interleukin 6 (interferon, beta 2) Extracellular Space cytokine 1.034 KLF2 Kruppel-like factor 2 (lung) Nucleus transcription regulator 1.084 LECT1 leukocyte cell derived chemotaxin 1 Extracellular Space other 1.062 LINC00473 long intergenic non-protein coding RNA 473 unknown other 1.097 LOC100129775 uncharacterized LOC100129775 unknown other 1.047 LOC100505890 uncharacterized LOC100505890 unknown other 1.025 LOC100506206 uncharacterized LOC100506206 unknown other 1.192 LOC100506236 uncharacterized LOC100506236 unknown other 1.126 LOC100507492 uncharacterized LOC100507492 unknown other 1.086 LOC100507520 uncharacterized L0C100507520 unknown other 1.495 LOC285740 uncharacterized LOC285740 unknown other 1.027 LOC389043 uncharacterized LOC389043 unknown other 1.330 LOC400752 uncharacterized LOC400752 unknown other 1.115 LOC401317 uncharacterized LOC401317 unknown other 1.034 LOC728724 hCG1814486 unknown other 1.051 LOXL4 lysyl oxidase-like 4 Extracellular Space enzyme 1.122 LUM lumican Extracellular Space other 1.073 LYPD2 LY6/PLAUR domain containing 2 unknown other 1.101 MAPK4 mitogen-activated protein kinase 4 Cytoplasm kinase 1.103 MFAP5 microfibrillar associated protein 5 Extracellular Space other 1.024 MGC24103 uncharacterized MGC24103 unknown other 1.045 MGC39545 uncharacterized LOC403312 unknown other 1.026 MOXD1 monooxygenase, DBH-like 1 Cytoplasm enzyme 1.124 MYF6 myogenic factor 6 (herculin) Nucleus transcription regulator 1.127 NCKAP1 NCK-associated protein 1 Plasma Membrane other 1.043 NR3C1 nuclear receptor subfamily 3, group C, member 1 Nucleus ligand-dependent 1.058 (glucocorticoid receptor) nuclear receptor NTSR1 neurotensin receptor 1 (high affinity) Plasma Membrane G-protein coupled 1.058 receptor OR52B2 olfactory receptor, family 52, subfamily B, member 2 Plasma Membrane G-protein coupled 1.051 receptor OTOGL otogelin-like unknown other 1.039 PAOX polyamine oxidase (exo-N4-amino) Cytoplasm enzyme 1.043 PBX1 pre-B-cell leukemia homeobox 1 Nucleus transcription regulator 1.021 PHLDA3 pleckstrin homology-like domain, family A, member 3 Plasma Membrane other 1.056 PIM1 pim-1 oncogene Cytoplasm kinase 1.041 PLD4 phospholipase D family, member 4 unknown enzyme 1.087 POU4F2 POU class 4 homeobox 2 Nucleus transcription regulator 1.040 PRKCH protein kinase C, eta Cytoplasm kinase 1.169 PRODH2 proline dehydrogenase (oxidase) 2 Cytoplasm enzyme 1.056 PVRL3 poliovirus receptor-related 3 Plasma Membrane other 1.064 RELN reelin Extracellular Space peptidase 1.113 RHO rhodopsin Plasma Membrane G-protein coupled 1.024 receptor RHOT1 ras homolog family member T1 Cytoplasm enzyme 1.029 RPS6KB2 ribosomal protein S6 kinase, 70 kDa, polypeptide 2 Cytoplasm kinase 1.077 RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin Nucleus transcription regulator 1.053 D-related) SEMA4C sema domain, immunoglobulin domain (Ig), transmembrane Plasma Membrane other 1.135 domain (TM) and short cytoplasmic domain, (semaphorin) 4C SEMA5A sema domain, seven thrombospondin repeats (type 1 and Plasma Membrane transmembrane 1.092 type 1-like), transmembrane domain (TM) and short receptor cytoplasmic domain, (semaphorin) 5A SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), Extracellular Space other 1.030 member 1 SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen Extracellular Space other 1.091 activator inhibitor type 1), member 1 SHE Src homology 2 domain containing E Cytoplasm other 1.030 SLC18A3 solute carrier family 18 (vesicular acetylcholine), member 3 Plasma Membrane transporter 1.056 SLC22A18 solute carrier family 22, member 18 Plasma Membrane transporter 1.173 SLC22A7 solute carrier family 22 (organic anion transporter), member 7 Plasma Membrane transporter 1.077 SLC38A3 solute carrier family 38, member 3 Plasma Membrane transporter 1.033 SMAD3 SMAD family member 3 Nucleus transcription regulator 1.042 STARD13 StAR-related lipid transfer (START) domain containing 13 Cytoplasm other 1.269 TM4SF4 transmembrane 4 L six family member 4 Plasma Membrane other 1.024 TNFRSF10C tumor necrosis factor receptor superfamily, member 10c, Plasma Membrane transmembrane 1.030 decoy without an intracellular domain receptor TRIB1 tribbles homolog 1 (Drosophila) Cytoplasm kinase 1.041 TRPV1 transient receptor potential cation channel, subfamily V, Plasma Membrane ion channel 1.037 member 1 TTC18 tetratricopeptide repeat domain 18 unknown other 1.072 UCA1 urothelial cancer associated 1 (non-protein coding) unknown other 1.041 WFDC9 WAP four-disulfide core domain 9 Extracellular Space other 1.052 XRN1 5′-3′ exoribonuclease 1 Cytoplasm enzyme 1.027 ZADH2 zinc binding alcohol dehydrogenase domain containing 2 Cytoplasm enzyme 1.129 ZBTB20 zinc finger and BTB domain containing 20 Nucleus other 1.044

TABLE 3 Rapamycin-sensitive genes differentially regulated in brain of Alzheimer's disease patients with advanced disease (178 known genes) Symbol Entrez Gene Name Location Type(s) Fold Change ABLIM2 actin binding LIM protein family, member 2 Cytoplasm other 0.905 ABTB1 ankyrin repeat and BTB (POZ) domain containing 1 Cytoplasm translation regulator 1.058 ACSL6 acyl-CoA synthetase long-chain family member 6 Cytoplasm enzyme 0.937 ACTRT1 actin-related protein T1 Cytoplasm other 1.025 ACVR2B activin A receptor, type IIB Plasma Membrane kinase 1.038 ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 Extracellular Space peptidase 1.082 motif, 2 ADAMTSL5 ADAMTS-like 5 Extracellular Space other 1.094 AHNAK2 AHNAK nucleoprotein 2 unknown other 1.056 ANKRD36BP2 ankyrin repeat domain 36B pseudogene 2 unknown other 0.913 AP1S1 adaptor-related protein complex 1, sigma 1 subunit Cytoplasm transporter 0.955 ATAD3A/ATAD3B ATPase family, AAA domain containing 3A Nucleus other 1.078 ATF7IP activating transcription factor 7 interacting protein Nucleus transcription regulator 0.934 ATRNL1 attractin-like 1 unknown other 0.865 BARX2 BARX homeobox 2 Nucleus transcription regulator 1.080 BCOR BCL6 corepressor Nucleus transcription regulator 1.032 BMP7 bone morphogenetic protein 7 Extracellular Space growth factor 1.046 BPI bactericidal/permeability-increasing protein Plasma Membrane transporter 1.036 BTNL9 butyrophilin-like 9 unknown other 1.063 C17orf99 chromosome 17 open reading frame 99 unknown other 1.039 C18orf26 chromosome 18 open reading frame 26 unknown other 0.960 C1orf127 chromosome 1 open reading frame 127 unknown other 1.087 C3orf80 chromosome 3 open reading frame 80 unknown other 0.952 CACNA1D calcium channel, voltage-dependent, L type, alpha 1D Plasma Membrane ion channel 1.070 subunit CARD14 caspase recruitment domain family, member 14 Cytoplasm other 1.025 CC2D2A coiled-coil and C2 domain containing 2A unknown other 1.098 CCL1 chemokine (C-C motif) ligand 1 Extracellular Space cytokine 1.063 CCL11 chemokine (C-C motif) ligand 11 Extracellular Space cytokine 1.039 CCL2 chemokine (C-C motif) ligand 2 Extracellular Space cytokine 1.082 CCNB2 cyclin B2 Cytoplasm other 1.073 CCR1 chemokine (C-C motif) receptor 1 Plasma Membrane G-protein coupled 1.032 receptor CEACAM1 carcinoembryonic antigen-related cell adhesion molecule Plasma Membrane transmembrane 1.081 (includes others) 1 (biliary glycoprotein) receptor CEP68 centrosomal protein 68 kDa Cytoplasm other 1.040 CLU clusterin Extracellular Space other 0.911 CPLX2 complexin 2 Cytoplasm other 0.918 CPXM2 carboxypeptidase X (M14 family), member 2 Extracellular Space peptidase 1.030 CREB3L4 cAMP responsive element binding protein 3-like 4 Nucleus transcription regulator 1.054 CRP C-reactive protein, pentraxin-related Extracellular Space other 1.111 CTDSP1 CTD (carboxy-terminal domain, RNA polymerase II, Nucleus phosphatase 1.119 polypeptide A) small phosphatase 1 CUX1 cut-like homeobox 1 Nucleus transcription regulator 0.969 DCAF12L1 DDB1 and CUL4 associated factor 12-like 1 unknown other 1.038 DCD dermcidin Extracellular Space other 1.152 DCLK1 doublecortin-like kinase 1 Plasma Membrane kinase 0.939 DLG2 discs, large homolog 2 (Drosophila) Plasma Membrane kinase 0.917 DNAH6 dynein, axonemal, heavy chain 6 unknown other 0.957 DRP2 dystrophin related protein 2 Plasma Membrane other 1.038 DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1 Cytoplasm other 0.946 DZIP3 DAZ interacting protein 3, zinc finger Cytoplasm enzyme 0.905 EBF2 early B-cell factor 2 Nucleus other 1.024 EIF4E eukaryotic translation initiation factor 4E Cytoplasm translation regulator 0.920 ELAVL4 ELAV (embryonic lethal, abnormal vision, Drosophila)-like Cytoplasm other 0.931 4 (Hu antigen D) ENTPD8 ectonucleoside triphosphate diphosphohydrolase 8 unknown enzyme 1.063 FAM155A family with sequence similarity 155, member A unknown other 0.860 FAM171B family with sequence similarity 171, member B unknown other 0.948 FAM64A family with sequence similarity 64, member A Nucleus other 1.154 FAT3 FAT tumor suppressor homolog 3 (Drosophila) unknown other 0.954 FGF11 fibroblast growth factor 11 Extracellular Space growth factor 1.185 FJX1 four jointed box 1 (Drosophila) Extracellular Space other 1.104 FLJ35946 uncharacterized protein FLJ35946 unknown other 1.137 FN3K fructosamine 3 kinase Cytoplasm kinase 1.269 GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2 Plasma Membrane G-protein coupled 0.862 receptor GALNT10 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N- Cytoplasm enzyme 1.064 acetylgalactosaminyltransferase 10 (GalNAc-T10) GFAP glial fibrillary acidic protein Cytoplasm other 1.091 GIGYF1 GRB10 interacting GYF protein 1 unknown other 1.042 GLI2 GLI family zinc finger 2 Nucleus transcription regulator 1.033 GLRA1 glycine receptor, alpha 1 Plasma Membrane ion channel 1.043 GNG8 guanine nucleotide binding protein (G protein), gamma 8 Plasma Membrane enzyme 1.059 GPM6A glycoprotein M6A Plasma Membrane ion channel 0.920 GPR176 G protein-coupled receptor 176 Plasma Membrane G-protein coupled 1.098 receptor GSG1L GSG1-like unknown other 1.025 HCAR3 hydroxycarboxylic acid receptor 3 Plasma Membrane G-protein coupled 1.053 receptor HDAC5 histone deacetylase 5 Nucleus transcription regulator 1.125 HHIPL1 HHIP-like 1 unknown other 1.063 HIST1H4A histone cluster 1, H4a Nucleus other 0.894 (includes others) HMGCS2 3-hydroxy-3-methylglutaryl-CoA synthase 2 Cytoplasm enzyme 1.034 (mitochondrial) HOXD10 homeobox D10 Nucleus transcription regulator 1.038 HYDIN HYDIN, axonemal central pair apparatus protein unknown other 1.090 IL1RAPL1 interleukin 1 receptor accessory protein-like 1 Plasma Membrane transmembrane 1.029 receptor IL6 interleukin 6 (interferon, beta 2) Extracellular Space cytokine 1.037 IRS2 insulin receptor substrate 2 Cytoplasm enzyme 0.925 IRS2 insulin receptor substrate 2 Cytoplasm enzyme 0.941 IRX4 iroquois homeobox 4 Nucleus transcription regulator 1.032 ITGBL1 integrin, beta-like 1 (with EGF-like repeat domains) unknown other 1.038 KCNAB1 potassium voltage-gated channel, shaker-related Plasma Membrane ion channel 0.936 subfamily, beta member 1 KCND2 potassium voltage-gated channel, Shal-related subfamily, Plasma Membrane ion channel 0.958 member 2 KCNG4 potassium voltage-gated channel, subfamily G, member 4 Plasma Membrane ion channel 1.152 KIAA1683 KIAA1683 Cytoplasm other 1.046 KLF2 Kruppel-like factor 2 (lung) Nucleus transcription regulator 1.103 KRTAP9-2 keratin associated protein 9-2 unknown other 1.022 LECT1 leukocyte cell derived chemotaxin 1 Extracellular Space other 1.060 LINC00473 long intergenic non-protein coding RNA 473 unknown other 1.085 LOC100129775 uncharacterized LOC100129775 unknown other 1.051 LOC100287803 uncharacterized LOC100287803 unknown other 0.854 LOC100506206 uncharacterized LOC100506206 unknown other 1.199 LOC100506236 uncharacterized LOC100506236 unknown other 1.127 LOC100507492 uncharacterized LOC100507492 unknown other 1.080 LOC100507520 uncharacterized LOC100507520 unknown other 1.497 LOC285740 uncharacterized LOC285740 unknown other 1.024 LOC389043 uncharacterized LOC389043 unknown other 1.255 LOC400752 uncharacterized LOC400752 unknown other 1.113 LOC401317 uncharacterized LOC401317 unknown other 1.037 LOC728323 uncharacterized LOC728323 unknown other 0.921 LOC728724 hCG1814486 unknown other 1.070 LOXL4 lysyl oxidase-like 4 Extracellular Space enzyme 1.136 LRRC71 leucine rich repeat containing 71 unknown other 1.052 LUM lumican Extracellular Space other 1.069 LYPD2 LY6/PLAUR domain containing 2 unknown other 1.102 MAPK1 mitogen-activated protein kinase 1 Cytoplasm kinase 0.912 MAPK4 mitogen-activated protein kinase 4 Cytoplasm kinase 1.100 MBD3L2 (includes methyl-CpG binding domain protein 3-like 2 unknown other 1.025 others) MCTP1 multiple C2 domains, transmembrane 1 unknown other 0.914 MECOM MDS1 and EVI1 complex locus Nucleus transcription regulator 1.024 MFAP5 microfibrillar associated protein 5 Extracellular Space other 1.026 MGC24103 uncharacterized MGC24103 unknown other 1.050 MMP16 matrix metallopeptidase 16 (membrane-inserted) Extracellular Space peptidase 0.928 MOXD1 monooxygenase, DBH-like 1 Cytoplasm enzyme 1.103 MYF6 myogenic factor 6 (herculin) Nucleus transcription regulator 1.136 NAV2 neuron navigator 2 Nucleus other 1.037 NCKAP1 NCK-associated protein 1 Plasma Membrane other 1.043 NHSL1 NHS-like 1 unknown other 0.960 NR3C1 nuclear receptor subfamily 3, group C, member 1 Nucleus ligand-dependent 1.078 (glucocorticoid receptor) nuclear receptor NTSR1 neurotensin receptor 1 (high affinity) Plasma Membrane G-protein coupled 1.053 receptor OIP5-AS1 OIP5 antisense RNA 1 (non-protein coding) unknown other 0.888 OR52B2 olfactory receptor, family 52, subfamily B, member 2 Plasma Membrane G-protein coupled 1.065 receptor OTOGL otogelin-like unknown other 1.031 PEX5L peroxisomal biogenesis factor 5-like Cytoplasm ion channel 0.932 PHLDA3 pleckstrin homology-like domain, family A, member 3 Plasma Membrane other 1.067 PIM1 pim-1 oncogene Cytoplasm kinase 1.054 PLD4 phospholipase D family, member 4 unknown enzyme 1.085 POU4F2 POU class 4 homeobox 2 Nucleus transcription regulator 1.034 PRKCH protein kinase C, eta Cytoplasm kinase 1.156 PRODH2 proline dehydrogenase (oxidase) 2 Cytoplasm enzyme 1.062 PVRL3 poliovirus receptor-related 3 Plasma Membrane other 1.066 PYCR1 pyrroline-5-carboxylate reductase 1 Cytoplasm enzyme 1.048 RAB3C (includes RAB3C, member RAS oncogene family Cytoplasm enzyme 0.941 EG:115827) RELN reelin Extracellular Space peptidase 1.081 RMI2 RMI2, RecQ mediated genome instability 2, homolog (S. cerevisiae) unknown other 1.069 RND3 Rho family GTPase 3 Cytoplasm enzyme 1.026 RNF128 ring finger protein 128, E3 ubiquitin protein ligase Cytoplasm enzyme 0.952 RPS6KB2 ribosomal protein S6 kinase, 70 kDa, polypeptide 2 Cytoplasm kinase 1.098 RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin Nucleus transcription regulator 1.055 D-related) SCGN secretagogin, EF-hand calcium binding protein Cytoplasm other 1.037 SCN8A sodium channel, voltage gated, type VIII, alpha subunit Plasma Membrane ion channel 0.924 SEMA4C sema domain, immunoglobulin domain (Ig), Plasma Membrane other 1.146 transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C SEMA5A sema domain, seven thrombospondin repeats (type 1 and Plasma Membrane transmembrane 1.083 type 1-like), transmembrane domain (TM) and short receptor cytoplasmic domain, (semaphorin) 5A SERPINA10 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, Extracellular Space other 1.029 antitrypsin), member 10 SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), Extracellular Space other 1.036 member 1 SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen Extracellular Space other 1.093 activator inhibitor type 1), member 1 SHE Src homology 2 domain containing E Cytoplasm other 1.043 SLC18A3 solute carrier family 18 (vesicular acetylcholine), member 3 Plasma Membrane transporter 1.056 SLC22A18 solute carrier family 22, member 18 Plasma Membrane transporter 1.176 SLC22A7 solute carrier family 22 (organic anion transporter), Plasma Membrane transporter 1.082 member 7 SLC25A27 solute carrier family 25, member 27 Cytoplasm transporter 0.952 SLC38A3 solute carrier family 38, member 3 Plasma Membrane transporter 1.046 SLITRK1 SLIT and NTRK-like family, member 1 unknown other 0.917 SLITRK1 SLIT and NTRK-like family, member 1 unknown other 0.948 SMAD3 SMAD family member 3 Nucleus transcription regulator 1.042 SORBS2 sorbin and SH3 domain containing 2 Plasma Membrane other 0.961 STAG3L1 stromal antigen 3-like 1 unknown other 1.088 STARD13 StAR-related lipid transfer (START) domain containing 13 Cytoplasm other 1.221 STX1B syntaxin 1B Plasma Membrane ion channel 0.915 SYCP3 synaptonemal complex protein 3 Nucleus other 1.023 TAOK1 TAO kinase 1 Cytoplasm kinase 0.965 TGM4 transglutaminase 4 (prostate) Extracellular Space enzyme 1.086 TIMM17B translocase of inner mitochondrial membrane 17 homolog Cytoplasm transporter 1.035 B (yeast) TMEM56 transmembrane protein 56 unknown other 0.947 TNFRSF10C tumor necrosis factor receptor superfamily, member 10c, Plasma Membrane transmembrane 1.028 decoy without an intracellular domain receptor TP73 tumor protein p73 Nucleus transcription regulator 1.045 TRPV1 transient receptor potential cation channel, subfamily V, Plasma Membrane ion channel 1.032 member 1 TSC2 tuberous sclerosis 2 Cytoplasm other 1.045 UCA1 urothelial cancer associated 1 (non-protein coding) unknown other 1.040 VEGFA vascular endothelial growth factor A Extracellular Space growth factor 1.090 VSNL1 visinin-like 1 Cytoplasm other 0.848 WFDC11 WAP four-disulfide core domain 11 Extracellular Space other 1.030 XRN1 5′-3′ exoribonuclease 1 Cytoplasm enzyme 1.023 YPEL1 yippee-like 1 (Drosophila) Nucleus enzyme 0.934 ZADH2 zinc binding alcohol dehydrogenase domain containing 2 Cytoplasm enzyme 1.133 ZBTB20 zinc finger and BTB domain containing 20 Nucleus other 1.052 ZC3H6 zinc finger CCCH-type containing 6 unknown other 0.928

TABLE 4 Rapamycin-sensitive genes differentially regulated in brain of Alzheimer's disease patients with mild disease - new targets Symbol Entrez Gene Name Location Type(s) Fold Change ABTB1 ankyrin repeat and BTB (POZ) domain containing 1 Cytoplasm translation regulator 1.057 AHNAK2 AHNAK nucleoprotein 2 unknown other 1.056 BARX2 BARX homeobox 2 Nucleus transcription regulator 1.077 BTNL9 butyrophilin-like 9 unknown other 1.056 CACNA1D calcium channel, voltage-dependent, L type, alpha 1D Plasma Membrane ion channel 1.063 subunit CARD14 caspase recruitment domain family, member 14 Cytoplasm other 1.034 CC2D2A coiled-coil and C2 domain containing 2A unknown other 1.102 CEP68 centrosomal protein 68 kDa Cytoplasm other 1.036 CPXM2 carboxypeptidase X (M14 family), member 2 Extracellular Space peptidase 1.026 CREB3L4 cAMP responsive element binding protein 3-like 4 Nucleus transcription regulator 1.064 CTDSP1 CTD (carboxy-terminal domain, RNA polymerase II, Nucleus phosphatase 1.098 polypeptide A) small phosphatase 1 DCAF12L1 DDB1 and CUL4 associated factor 12-like 1 unknown other 1.030 FAM64A family with sequence similarity 64, member A Nucleus other 1.214 FCGBP Fc fragment of IgG binding protein Extracellular Space other 1.057 FJX1 four jointed box 1 (Drosophila) Extracellular Space other 1.123 FN3K fructosamine 3 kinase Cytoplasm kinase 1.258 GLI2 GLI family zinc finger 2 Nucleus transcription regulator 1.032 GLRA1 glycine receptor, alpha 1 Plasma Membrane ion channel 1.041 GPR176 G protein-coupled receptor 176 Plasma Membrane G-protein coupled 1.092 receptor HHIPL1 HHIP-like 1 unknown other 1.057 HOXD10 homeobox D10 Nucleus transcription regulator 1.024 HYDIN HYDIN, axonemal central pair apparatus protein unknown other 1.077 KLF2 Kruppel-like factor 2 (lung) Nucleus transcription regulator 1.084 MFAP5 microfibrillar associated protein 5 Extracellular Space other 1.024 PHLDA3 pleckstrin homology-like domain, family A, member 3 Plasma Membrane other 1.056 POU4F2 POU class 4 homeobox 2 Nucleus transcription regulator 1.040 RHO rhodopsin Plasma Membrane G-protein coupled 1.024 receptor RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin Nucleus transcription regulator 1.053 D-related) STARD13 StAR-related lipid transfer (START) domain containing 13 Cytoplasm other 1.269 TRIB1 tribbles homolog 1 (Drosophila) Cytoplasm kinase 1.041

TABLE 5 Rapamycin-sensitive genes differentially regulated in brain of Alzheimer's disease patients with advanced disease - new targets Fold Symbol Entrez Gene Name Location Type(s) Change ABLIM2 actin binding LIM protein family, member 2 Cytoplasm other 0.905 ABTB1 ankyrin repeat and BTB (POZ) domain containing 1 Cytoplasm translation regulator 1.058 ACSL6 acyl-CoA synthetase long-chain family member 6 Cytoplasm enzyme 0.937 ACTRT1 actin-related protein T1 Cytoplasm other 1.025 AHNAK2 AHNAK nucleoprotein 2 unknown other 1.056 AP1S1 adaptor-related protein complex 1, sigma 1 subunit Cytoplasm transporter 0.955 ATAD3A/ATAD3B ATPase family, AAA domain containing 3A Nucleus other 1.078 ATF7IP activating transcription factor 7 interacting protein Nucleus transcription regulator 0.934 ATRNL1 attractin-like 1 unknown other 0.865 BARX2 BARX homeobox 2 Nucleus transcription regulator 1.080 BCOR BCL6 corepressor Nucleus transcription regulator 1.032 BTNL9 butyrophilin-like 9 unknown other 1.063 CACNA1D calcium channel, voltage-dependent, L type, alpha 1D Plasma Membrane ion channel 1.070 subunit CARD14 caspase recruitment domain family, member 14 Cytoplasm other 1.025 CC2D2A coiled-coil and C2 domain containing 2A unknown other 1.098 CEP68 centrosomal protein 68 kDa Cytoplasm other 1.040 CPXM2 carboxypeptidase X (M14 family), member 2 Extracellular Space peptidase 1.030 CREB3L4 cAMP responsive element binding protein 3-like 4 Nucleus transcription regulator 1.054 CTDSP1 CTD (carboxy-terminal domain, RNA polymerase II, Nucleus phosphatase 1.119 polypeptide A) small phosphatase 1 DCLK1 doublecortin-like kinase 1 Plasma Membrane kinase 0.939 DLG2 discs, large homolog 2 (Drosophila) Plasma Membrane kinase 0.917 DNAH6 dynein, axonemal, heavy chain 6 unknown other 0.957 DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1 Cytoplasm other 0.946 DZIP3 DAZ interacting protein 3, zinc finger Cytoplasm enzyme 0.905 ELAVL4 ELAV (embryonic lethal, abnormal vision, Drosophila)-like Cytoplasm other 0.931 4 (Hu antigen D) FAM155A family with sequence similarity 155, member A unknown other 0.860 FAM64A family with sequence similarity 64, member A Nucleus other 1.154 FAT3 FAT tumor suppressor homolog 3 (Drosophila) unknown other 0.954 FJX1 four jointed box 1 (Drosophila) Extracellular Space other 1.104 FN3K fructosamine 3 kinase Cytoplasm kinase 1.269 GABBR2 gamma-aminobutyric acid (GABA) B receptor, 2 Plasma Membrane G-protein coupled 0.862 receptor GALNT10 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N- Cytoplasm enzyme 1.064 acetylgalactosaminyltransferase 10 (GalNAc-T10) GLI2 GLI family zinc finger 2 Nucleus transcription regulator 1.033 GLRA1 glycine receptor, alpha 1 Plasma Membrane ion channel 1.043 GPR176 G protein-coupled receptor 176 Plasma Membrane G-protein coupled 1.098 receptor GSG1L GSG1-like unknown other 1.025 HHIPL1 HHIP-like 1 unknown other 1.063 HOXD10 homeobox D10 Nucleus transcription regulator 1.038 HYDIN HYDIN, axonemal central pair apparatus protein unknown other 1.090 IRX4 iroquois homeobox 4 Nucleus transcription regulator 1.032 KLF2 Kruppel-like factor 2 (lung) Nucleus transcription regulator 1.103 KRTAP9-2 keratin associated protein 9-2 unknown other 1.022 MBD3L2 (includes methyl-CpG binding domain protein 3-like 2 unknown other 1.025 others) MCTP1 multiple C2 domains, transmembrane 1 unknown other 0.914 MFAP5 microfibrillar associated protein 5 Extracellular Space other 1.026 MMP16 matrix metallopeptidase 16 (membrane-inserted) Extracellular Space peptidase 0.928 PEX5L peroxisomal biogenesis factor 5-like Cytoplasm ion channel 0.932 PHLDA3 pleckstrin homology-like domain, family A, member 3 Plasma Membrane other 1.067 POU4F2 POU class 4 homeobox 2 Nucleus transcription regulator 1.034 PYCR1 pyrroline-5-carboxylate reductase 1 Cytoplasm enzyme 1.048 RND3 Rho family GTPase 3 Cytoplasm enzyme 1.026 RNF128 ring finger protein 128, E3 ubiquitin protein ligase Cytoplasm enzyme 0.952 RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin Nucleus transcription regulator 1.055 D-related) SLITRK1 SLIT and NTRK-like family, member 1 unknown other 0.917 SLITRK1 SLIT and NTRK-like family, member 1 unknown other 0.948 SORBS2 sorbin and SH3 domain containing 2 Plasma Membrane other 0.961 STAG3L1 stromal antigen 3-like 1 unknown other 1.088 STARD13 StAR-related lipid transfer (START) domain containing 13 Cytoplasm other 1.221 STX1B syntaxin 1B Plasma Membrane ion channel 0.915 TGM4 transglutaminase 4 (prostate) Extracellular Space enzyme 1.086 TMEM56 transmembrane protein 56 unknown other 0.947 WFDC11 WAP four-disulfide core domain 11 Extracellular Space other 1.030 YPEL1 yippee-like 1 (Drosophila) Nucleus enzyme 0.934

The invention will now be further understood with reference to the following non-limiting examples.

EXAMPLES Example 1 Gene Expression Microarray Analysis of Brain Samples from Alzheimer's Disease Patients

1.1 Patients and Biomaterials

Human brain tissue collected by the Oxford Project to Investigate Memory and Aging (OPTIMA) was made available through the Thomas Willis brain bank. In total, samples from 252 brains were available from a mix of elderly controls and patients suffer from preclinical, mild and severe AD at the time of death (as determined by Braak staging). The number of cases included in the study was based on availability, not statistical power calculations, as the outcome, and hence number of patients in each group-of-interest, was unknown. The tissue was snap frozen at the time of autopsy: and available from the lateral temporal lobe (severely affected by AD pathology), frontal lobe (affected by AD pathology) and occipital lobe (largely unaffected by AD pathology). A wealth of clinical information was available about each patient, including: Braak stage (severity of AD); additional pathology; age of onset and age at death; personal and family history of cancer; plasma homocysteine levels, and the results of annual clinical tests including test of cognitive performance (CAMCOG).

1.2 DNA, RNA and Protein Extraction

RNA, DNA and protein were isolated from lateral temporal, frontal and occipital lobe tissue of each patient by TRI-reagent extraction. 100 mg of frozen tissue was homogenised in 1 ml TRI-reagent, incubated at room temperature (RT) for 5 minutes, and supplemented with 100 μl 1-bromo-3-chloropropane. The solution was vigorously mixed for 15 seconds, incubated for 2 minutes, and centrifuged at 12,000 rotational centrifugal force (g) for 15 minutes at 4° C. to separate the RNA, DNA and protein layers.

The aqueous RNA layer was transferred to an eppendorf, supplemented with 500 μl isopropanol and mixed gently by inversion. After five minute incubation, the solution was centrifuged at 12,000 g for 8 minutes at 4° C. The pellet was washed in 1 ml 75% ethanol, centrifuged at 7,500 g for 5 minutes at 4° C., and ethanol wash removed. The pellet was air-dried for 30 minutes and rehydrated in 100 μl nuclease free water by incubation at 55° C. for 15 minutes, prior to storage at −80° C.

RNA was converted to cDNA by reverse transcription: 50 μl of 200 ng/μl RNA was added to 50 μl of Reverse Transcriptase master mix (composed of 10 μl 10×reverse transcriptase buffer; 4 μl dNTP mix (100 mM); 10 μl random primers; 5 μl MultiScribe Reverse Transcriptase (50 U/μl); and 21 μl nuclease free water), and incubated at 25° C. for 10 minutes; 37° C. for 120 minutes and 85° C. for 5 seconds in a Thermal cycler. The cDNA was precipitated with isopropanol (100 μl cDNA supplemented with 20 μl of 3M sodium citrate at pH 5 and 400 μl isopropanol), centrifuged at high speed for 10 minutes, and the resulting pellet washed in ice cold 100% ethanol. Following high speed centrifugation and supernatant removal, the pellet was air dried overnight, and rehydrated in 100 μl nuclease free water, prior to storage at 4° C.

The remaining TRI-reagent layers were supplemented with 300 μl ethanol and centrifuged at 12,000 g for 5 minutes at 4° C. to produce the DNA pellet. The pink supernatant was transferred to a clean eppendorf in preparation for protein extraction. The DNA pellet was washed three times, 1 hour per wash, in 0.1M sodium citrate in 10% ethanol, with centrifugation at 12,000 g for 5 minutes between washes. Following a 30 minute wash in 75% ethanol, the pellet was centrifuged at 2,000 g for 5 minutes to allow wash removal, and the pellet air dried overnight. The pellet was dissolved in nuclease free water for 24 hours, centrifuged at 16,000 g for 10 minutes, and supernatant transferred to a clean tube to separate DNA from any insoluble material. The DNA was stored at 4° C.

The protein was precipitated from the pink layer by 15 minute incubation with 3 volumes acetone prior to centrifugation at 12,000 g for 10 min at 4° C. The protein pellet was subjected to three 10 minute washes in 0.3M guanidine hydrochloride in 95% ethanol and 2.5% glycerol, and dissolved in radio-immunoprecipitation (RIPA) buffer (composition: 0.1M sodium chloride, 0.01M Tris hydrochloride, 1:500 EDTA, 400 ug/ml phenylmethanesulfonylfluoride, 2 ug/ml aprotinin and 1% sodium dodecyl sulphate). The protein was stored at −20° C.

1.3 One-Colour Custom Microarray Based Gene Expression Analysis (Agilent)

8×15K Custom Microarrays (Agilent Technologies: able to accommodate up to 15,000 genes) were designed to include various housekeeping genes (719 genes), internal controls (3141 genes), and genes that were differentially expressed in AD brain relative to control brain based on a published dataset (Xu, P. T. et al. Differences in apolipoprotein E3/3 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Neurobiol. Dis. 21, 256-275 (2006); Xu, P. T. et al. A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease. Mol. Cell Neurosci. 36, 313-331 (2007) (3718 genes). The remaining 7422 spaces were filled with known rapamycin-regulated genes (based on an IPA Ingenuity search) and the genes that were identified as rapamycin-regulated in lymphocytes based on two-colour microarray based gene expression analysis.

Of the 252 patients for whom tissue was available through the Thomas Willis brain bank, 32 patients were selected for one-colour custom microarray based gene expression analysis. They included control subjects and patients with mild and advanced AD. The exclusion criteria were as follows: vascular disease; Parkinson's disease; ApoE ε2/ε2, ApoE ε2/ε3 and ApoE ε4/ε4 genotypes (not enough patients for meaningful statistical analysis); and high plasma homocysteine level (>35 μM).

1.3.1 Sample Preparation

RNA was extracted from the frontal lobe of each subject by TRI-reagent protocol as described in 1.2. The RNA was treated with DNase. The suitability of the RNA for microarray based gene expression analysis was determined by Agilent RNA nano-chip analysis. RIN values ranged from 2-3 indicating relatively poor quality RNA. However, this was unavoidable, as the source brain tissue had significant post-mortem time prior to freezing, resulting in inevitable degradation.

1.3.2 Conversion of RNA to Labelled cRNA

200 ng of RNA was converted to cDNA, and subsequently to labelled cRNA, with the low-input quick amplification labelling kit. The spike mix was incubated at 37° C. for 5 minutes, and diluted in the provided dilution buffer (Agilent Techologies) as shown in Table 6. 2 μl of the diluted spike mix was added to the RNA (200 ng) in a 1.5 μl volume. Cyanine 3-CTP was used to label all samples. The labelled and amplified cRNA samples were purified by standard Qiagen RNeasy mini column protocol, and quality assessed and quantified.

TABLE 6 Preparation of Spike Mix Starting amount of RNA Spike mix Total volume per RNA Concentration Serial dilutions labelling (ng) (ng/μl) First Second Third Fourth (μl) 200 133.3 1:20 1:25 1:10 2 1.3.3 Hybridisation

600 ng of labelled cRNA was added to various fragmentation components (Table 7), incubated at 60° C. for 30 minutes, and cooled on ice for 1 min. 25 μl of GEx Hybridisation buffer HI-RPM was added to stop fragmentation. The sample was gently mixed, centrifuged at 13,000 rpm for 1 min, and placed on ice in preparation for hybridisation. The microarray was assembled and incubated overnight: the Custom 8×15K Microarray was used and 40 μl of sample was added per 15K array. After 17 hour hybridisation, the microarrays were washed and scanned on the Agilent C Scanner on programme AgilentHD_GX_1 color, with the settings amended as shown in Table 8.

TABLE 7 Fragmentation components Volume/Mass (for 8 × 15K Components (Agilent) microarray) Cy3-labelled cRNA 600 ng 10 × blocking agent 5 μl Nuclease free water Bring total volume to 24 μl 25 × fragmentation buffer 1 μl Total volume 25 μl

TABLE 8 Microarray scanner settings for one-colour microarray based gene expression analysis (Agilent) 8 × 15K HD microarray format Dye Channel Green Scan region Scan area (61 × 21.6 mm) Scan resolution (μM) 5 Tiff 20 bit 1.3.4. Data Analysis

The feature extraction programme was used to collate the Custom Microarray layout with the output of the scanner. The results from individual patients were grouped based on subject diagnosis, disease severity (as defined by Braak stage) and ApoE genotype. For the purposes of this study, the groups-of-interest were as follows (see Table 9):

TABLE 9 Patient diagnosis ApoE genotype Number of patients Control (entorhinal ApoE ε3/ε3 5 stage) Mild AD (limbic ApoE ε3/ε3 5 stage) Advanced AD ApoE ε3/ε3 4 (neocortical stage) Advanced AD ApoE ε3/ε4 18 (neocortical stage)

Statistical Analysis of Microarray (SAM) was used to carry out unpaired, two-sample T tests for each gene in a group-of-interest compared to control. SAM identifies genes that are differentially expressed at RNA level in the group-of-interest compared to control group; the direction of expression; fold change; and an estimate of the false discovery rate (FDR). For the purpose of our study, we selected an estimated FDR of 10% as acceptable for identifying differentially expressed genes. SAM was carried out with 1000 permutations, and the output processed to remove duplicates. The output was analysed with the IPA Ingenuity software (www.ingenuity.com).

Tables 2 shows differentially expressed transcripts in brain from early AD patients (limbic stage) relative to control (entorhinal stage). Table 3 shows differentially expressed transcripts in brain from advanced AD patients (neocortical stage) relative to control (entorhinal stage).

Example 2 Q-PCR Validation of Microarray Results

Real-time PCR (Q-PCR) allows relative quantification of a gene-of-interest by calculating the expression of the gene relative to a housekeeping gene such as beta-actin, allowing patient to patient comparison. The validation study was carried out on cDNA obtained from the same patients and brain regions that were used for the microarray study. The genes were selected as they were shown to be either significantly up- or down-regulated in advanced AD (neocortical stage) compared to control in the microarray study. The Universal probe library design centre (Roche Diagnostic Website) was used to design Q-PCR systems for the genes (see Table 10); and primers and probes ordered from Sigma Genosys and Roche respectively.

TABLE 10 Roche probe, primer sequences, and optimal annealing temperature corresponding to each gene-of-interest Optimal annealing Roche Forward primer Backward primer temperature Gene Probe (5′-3′) (5′-3′) (° C.) Beta actin 24 TCAGCTGTGGGGTC GAAGGGGACAGGCAG 62 CTGT TGAG EIF4E 35 GATGGCGACTGTCG TGGGTTAGCAACCTC 60 (Variant 1 AACC CTGAT and 2) EIF4E 35 GTGTAGCGCACACT TGGGTTAGCAACCTC 60 (Variant 3) TTCTGG CTGAT MAPK1 62 CCGTGACCTCAAGC GCCAGGCCAAAGTCA 58 (Variant 1 CTTC CAG and 2) GABBR2 3 GCGAAGGACAGTGG GAGAGGGCGGATGGA 62 AGAAGT GATA SEMA4C 14 TTGTGCCGCGTAAG CAGCGTCAGTGTCAG 60 ACAGT GAAGT DZIP3 39 TGCCCAAGATCTGA CTCCAACACACCACC 60 TACAAGG GTACA SERPINE1 80 CTCCTGGTTCTGCC CAGGTTCTCTAGGGG 58 CAAGT CTTCC

For the composition of each 20 μl Q-PCR mix see Table 11. Two negative controls (water) and a cDNA standard curve (five serial dilutions starting with neat cDNA) were included per Q-PCR run. The samples were denatured at 96° C. for 15 minutes and amplified by 40 cycles of 96° C. for 15 seconds, optimal annealing temperature (Table 10) for 30 seconds and 72° C. for 30 seconds. FAM output was read in the annealing phase.

TABLE 11 Composition of Q-PCR reaction Manufacturer 0.5 μl Universal probe (10 μM) Roche 10 μl Absolute Q-PCR mix ThermoScientific (Compositition: 0.625 Units ThermoPrime Taq DNA polymerase, 75 mM Tris HCl (pH 8.8 at 25° C.), 20 mM (NH₄)₂SO₄, 1.5 mM MgCl₂, 0.01% (v/v) tween 20, 0.2 mM each of dATP, dCTP, dGTP, dTTP). 0.5 μl forward primer (20 μM) Sigma Genosys 0.5 μl backward primer (20 μM) Sigma Genosys 6.5 μl nuclease free water Qiagen 2 μl cDNA (neat, 1:4 and 1:16) Prepared as above 2.1 Data Analysis

Each of the cDNA standard curve serial dilutions were assigned an arbitrary copy number (1:1=10,000; 1:2=5,000; 1:4=2500; 1:8=1250; 1:16=625). The Rotor gene-6 programme automatically identifies the optimal threshold and determines the copy number of the gene-of-interest relative to the standard curve for each sample. The Q-PCR was considered fully optimised when the calculated standard curve copy number varied less than 10% from the assigned copy number. The values obtained for each gene were normalised to the corresponding beta-actin values to allow quantitative comparison of samples.

Example 2 Modulation of Rapamycin-Sensitive Genes has the Same Beneficial Effect on Alzheimer's Disease-Related Protein Expression as Rapamycin

2.1 Methods

The genes identified as rapamycin-sensitive genes (existing Table 1) were used for computer based (in silico) molecular network modelling and analysis (using the IPA molecular network tools). In silico simulation of molecular interactions in the AD brain was also carried out based on the expression pattern of the rapamycin-sensitive genes shown in Table 2. Selected rapamycin-sensitive genes were used for further simulations to predict the effect of silencing these rapamycin-sensitive genes on AD-related pathology.

The simulations were followed by experiments to verify whether the modulation of the downstream effectors of mTOR (rapamycin-sensitive genes) would lead to measureable changes in MAPT (microtubule associated protein tau) similar to rapamycin.

In the cellular models used, the mTOR activation is achieved by growth factors in the serum. The inhibition of mTOR by the addition of rapamycin counteracts this effect and reduces the production of AD-type phospho-tau in the cultures.

Cell Culture

SH-SY5Y human neuroblastoma cells were purchased from ECACC and cultured in DMEM/F-12 (Sigma) supplemented with 10% FCS Gold (PAA), 100 U penicillin-streptomycin (Invitrogen) and 2 mM L-glutamine (Sigma). Cells were kept in a humidified atmosphere at 37° C. and 5% CO₂. Cells were seeded in 96-well plates and cultured for 24 hours before siRNA treatment.

siRNA Treatment of SH-SY5Y Cells

siRNA was purchased from Origene and applied at 1 nM concentration for 48 hours. siRNA duplexes (Origene) were supplied as 20 μM stock solutions. siRNA was diluted in OPTIMEM to a 300 nM concentration and incubated at room temperature (RT) for 10 min. Lipofectamine (RNAiMAX) was also diluted in OPTIMEM and incubated at RT for 10 min. The lipofectamine mix and the duplex mix were added to the culture medium (antibiotic free) to achieve the final concentration of 1 nM siRNA and 0.3% lipofectamine. Cells were incubated at 37° C. for 4 hours, and then media was replaced with antibiotic free media until collection. Some cultures were treated with additional rapamycin for the last 24 hours of the culture period.

Immunostaining

Cells were sequentially fixed in Glyo-Fixx (Thermo Scientific) for 2 hours at RT and in 85% cold ethanol for 30 min. Blocking (of non-specific staining) was performed for 30 min at RT using 5% BSA and 0.1% Triton-X-100 in PBS. Cells were incubated with primary antibody overnight at 4° C. (for the negative controls, cells were incubated with PBS-Triton only). Cells were washed in PBS-0.1% Triton and incubated with secondary antibody (FITC conjugated) for 2 hours at 4° C. Cells were washed in PBS-0.1% Triton and propidium iodide counterstained. The antibodies used were mouse polyclonal to phospho-Tau (Abcam, 1:200) and anti-mouse IgG-FITC (Abcam, 1:400).

Propidium Iodide Staining

Cells were incubated with propidium iodide (Invitrogen, 10 μg/ml) supplemented with RNaseA (Sigma, 100 μg/ml) for 20 min at 37° C. and scanned.

Cytometry

Cytometry was performed using the Acumen Explorer TTP Lab Tech, Ltd. (Software version 3.1.12).

The propidium iodide staining was used to determine the cell cycle phase of the cells based on DNA content. It was measured using a 488 nm excitation laser triggering the 3° channel (bandpass filter 585-620 nm).

The immunostaining was used to measure the content of phospho-Tau in the cells. Measurement was carried out using a laser triggering the 1° channel (bandpass filter 500-530 nm).

Cell Cycle Analysis

To determine cut-offs for cells in different phases of the cell cycle, gate setting was performed based on the G1 and G2 peaks on the DNA content histogram. To determine the G1 and G2 peaks, the 3° total intensity in 20% histograms was analysed for each plate. Gates calculated were manually entered into the Acumen software.

The data exported and quantified included separately all cells and single cells. Single cells were further subcategorised into euploid, apoptotic and polyploid cells. Euploid cells were additionally classified into cells in G1S and G2M phases of the cell cycle.

Cellular Protein Measurement

The total fluorescence intensity from the 1° channel was used to compare total protein levels in the different cell populations defined above. Mean fluorescence intensity per cell (for the whole of the population) and mean fluorescence intensity per cell (for positive cells only) were analysed separately. Additionally the proportion of positive cells in each population was calculated.

2.2 Results

2.2.1 The Effects of Rapamycin

The in silico simulations (using the IPA molecular network modelling tool) indicated that the rapamycin regulated molecules interact with the AD-related proteins APP (amyloid precursor protein) and the microtubule associated protein tau (MAPT). The in silico analysis indicated that the activation of mTOR in normal circumstances would lead to the inhibition of MAPT and APP.

The gene expression patterns of rapamycin-sensitive genes in early stage AD patients (as shown in existing Table 2) were used to predict the activation state of APP and MAPT in the brain. Based on the expression pattern of rapamycin-sensitive genes in the early (limbic) stage of AD, the inhibition of MAPT and APP was predicted. The in silico simulation also predicted that this gene expression pattern is associated with the activation of mTOR. However, the expression pattern of many rapamycin-sensitive genes in the brain of AD patients is inconsistent with the known normal molecular interactions. This indicates that the AD-related deregulation of the mTOR pathway is also associated with unexpected variations from normal molecular interactions that are compatible with the idea that these molecules have variants (SNPs or other genetic variations) that interfere with their normal interactions.

The simulated inhibition of mTOR in this system (using rapamycin) will reverse the AD-associated inhibition of MAPT and APP, indicating that rapamycin could reverse the molecular expression changes seen in AD.

In the experimental paradigm mTOR is activated in the neuronal cells (in the presence of growth factors from the serum). The addition of rapamycin (100 ng/ml) will inhibit mTOR, leading to the down regulation of AD-related phospho-tau (p-tau) in the cells.

In the SH-SY5Y cellular model, p-tau expression was regulated in a cell-cycle dependent manner and protein content of cells was generally higher in the cells that were in the G2 phase of the cell cycle relative to cells in the G1 phase of the cell cycle (FIG. 1: White bars represent the G1 phase cell population; black bars represent the G2 phase population).

The effects of mTOR inhibition by rapamycin had the following effects. Firstly, the cell cycle kinetics were altered such that the G1 phase became longer and the G2 phase was shortened, as reflected by the accumulation of cells in the G1 phase of the cell cycle at the expense of the G2 phase (FIG. 2: Vertically shaded bars represent the G1 population; the horizontally shaded bars represent the G2 cell population. Lighter shades represent cells treated with Culture medium alone. Darker shades represent cells treated with Culture medium containing 100 ng/ml rapamycin. All data is normalised to Control (100%)). Secondly, the rapamycin induced a reduction of p-tau content in the whole cell culture. This is partly due to the alterations in cell cycle kinetics (reduction of the G2 cell population with the generally higher p-tau content). However, the rapamycin also had a cell cycle independent effect on p-tau leading to further reductions in this protein (FIG. 3: Grey bars represent all single cells; Vertically shaded bars represent the G1 population; the horizontally shaded bars represent the G2 cell population. Lighter shades represent cells treated with Culture medium alone. Darker shades represent cells treated with Culture medium containing 100 ng/ml rapamycin. All data are normalised to Control (100%)).

These findings indicate, in accordance with previous studies, that rapamycin is able to modulate the accumulation of AD-type p-tau both in a cell cycle dependent and independent manner.

The possibility that modulation of downstream effectors of mTOR (shown in Table 1) would have a similar effect to that observed with rapamycin was subsequently investigated.

2.2.2 CACNA1D

CACNA1D was not previously known to be a rapamycin-sensitive gene. Subsequently, the in silico molecular simulation of CACNA1D knockdown did not predict alteration in the expression of MAPT or APP.

However, the experimental data showed that the cell cycle effects of CACNA1D knock-down by siRNA were similar to that of rapamycin (FIG. 4: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA control and CACNA1D siRNA alone. Darker shades represent cells treated with an additional 100 ng/ml rapamycin. All data is normalised to Control (100%)). The effect of CACNA1D knock-down by siRNA did not alter the effect of rapamycin. This is consistent with the cell cycle modulator effect of CACNA1D downstream of mTOR.

Protein expression analysis indicated that the effect of CACNA1D knockdown is similar to that induced by rapamycin. However, the CACNA1D knockdown did not alter the effect of rapamycin on p-tau expression in cells (FIG. 5: Grey bars represent all single cells; Vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and CACNA1D siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)).

The data provide evidence that, contrary to prior knowledge, the CACNA1D gene expression is mTOR dependent. The data also provide evidence that modulation of CACNA1D has a similar effect to rapamycin in terms of cell cycle and AD-related p-tau expression.

The data provide evidence that the modulation of a downstream effector of mTOR has the same beneficial effect on AD-related cell cycle and protein changes as rapamycin.

2.2.3 GABBR2

The GABBR2 receptor has not previously been identified as a downstream effector of mTOR i.e. is not a known rapamycin-sensitive gene. Thus the in silico simulation of GABBR2 receptor knockdown did not predict a similar effect to rapamycin with respect to AD-related protein expression.

However, the effects of GABBR2 knockdown by siRNA in the experimental model were similar to that of rapamycin. The GABBR2 knockdown did not affect the rapamycin response significantly (FIG. 6: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA Control and GABBR2 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data is normalised to Control (100%)). These data are consistent with the cell cycle modulator effect of GABBR2 downstream of mTOR.

The effect of GABBR2 knockdown on p-tau expression was similar to that induced by rapamycin, albeit weaker. However, in the presence of rapamycin, GABBR2 knockdown had no further significant effect on p-tau expression in cells (FIG. 7: Grey bars represent all single cells; vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and GABBR2 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)).

The data provide evidence that, contrary to prior knowledge, the GABBR2 gene expression is mTOR dependent. The data also provide evidence that modulation of GABBR2 has a similar effect to rapamycin in terms of cell cycle and AD-related p-tau expression.

The data provides evidence that the modulation of a downstream effector of mTOR has the same beneficial effect on AD-related cell cycle and protein changes as rapamycin.

2.2.4 HOXD10

The HOXD10 gene was not previously known to be rapmycin-sensitive. Thus the in silico simulation of HOXD10 knockdown did not predict a similar effect to rapamycin with respect to AD-related protein expression.

In the experimental model, the siRNA to HOX10D did not affect the cell cycle in a similar fashion to rapamycin (FIG. 8: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA Control and HOX10D siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). However, rapamycin was able to exert its cell cycle modulator effect even when HOX10D was not expressed (FIG. 8). This would indicate that HOX10D does not play a role in the rapamycin induced cell cycle modulation.

HOX10D knockdown had a weak effect in reducing p-tau expression in the cellular model, mainly by reducing the amount of p-tau in the G1 cell population. The effects were significantly weaker than that of rapamycin and the HOXD10 knockdown did not affect the rapamycin effect (FIG. 9: Grey bars represent all single cells; Vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and HOX10D siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). The data provide evidence that the modulation of a downstream effector of mTOR has the same beneficial effect on AD-related protein changes as rapamycin.

2.2.5 KLF2

Although KLF2 was not previously identified as a rapamycin-sensitive gene, the indirect molecular interactions allowed the simulation of the effect of mTOR on KLF2. However, in AD the expression of KLF2 was found to be opposite to what would normally be expected in response to mTOR activation. The effects of KLF2 knockdown in the AD brain were simulated, and found to closely mimic the effects of rapamycin in terms of AD-related protein expression (MAPT and APP).

In the experimental model, the knockdown of KLF2 produced similar but weaker cell cycle effects relative to rapamycin. The KLF2 knockdown did not affect significantly the effect of rapamycin on the G1 phase of the cell cycle. However, the KLF2 knockdown led to a significant alteration of the G2 effect of rapamycin (FIG. 10: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA Control and KLF2 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). The data indicate that KLF2 is a downstream effector of the mTOR induced cell cycle response and it is essential for the G2 regulator effects of mTOR.

The effects of KLF2 knockdown on p-tau expression were similar to those of rapamycin, albeit a lot weaker. The KLF2 knockdown did not affect the rapamycin effect on p-tau expression (FIG. 11: Grey bars represent all single cells; Vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and KLF2 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)).

These data also indicate that the modulation of a rapamycin-sensitive gene will lead to effects that are similar to rapamycin.

2.2.6 RHO

RHO was not previously known to be a rapamycin-sensitive gene. However, the molecular interactions of RHO allowed the simulation of the effect of RHO knockdown in the AD brain. The in silico simulation indicated that RHO knockdown will lead to changes in the AD-related molecules (MAPT and APP) similar to that seen with Rapamycin.

In the experimental model the knockdown of RHO produced similar, but weaker cell cycle effects relative to rapamycin. The RHO knockdown did not affect significantly the effect of rapamycin on the G1 phase of the cell cycle. However, the RHO knockdown led to a significant alteration of the G2 effect of rapamycin (FIG. 12: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA Control and RHO siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). The data indicate that RHO is a downstream effector of the mTOR induced cell cycle response and it is essential for the G2 regulator effects of mTOR.

The effects of RHO knockdown on p-tau expression were similar to those of rapamycin, albeit a lot weaker. The RHO knockdown did not affect the rapamycin effect on p-tau expression (FIG. 13: Grey bars represent all single cells; Vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and RHO siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). These data are consistent with RHO acting downstream of mTOR.

The data also indicate that the modulation of a rapamycin-sensitive gene will lead to effects that are similar to rapamycin.

2.2.7 GLI2

Based on known molecular interactions it could be predicted in silico that GL12 (although not previously identified as a rapamycin-sensitive gene) would be differentially regulated by mTOR activation. The AD brain expression studies however indicated that the expression of GL12 is not consistent with the activation of mTOR. The in silico simulations carried out to predict the effects of GL12 knockdown in the AD brain indicated that the knockdown of GL12 would lead to effects that are very similar to that of rapamycin in terms of AD-related protein (MAPT and APP) expression in the brain.

The effects of GL12 knockdown by siRNA on the cell cycle were similar to that of rapamycin, but had no effect on rapamycin response (FIG. 14: Vertically shaded bars represent the cell population in the G1 phase of the cell cycle, and the G1 time; horizontally shaded bars represent the cells in the G2 phase of the cell cycle and the G2 time. Lighter shades represent cells treated with Culture medium, siRNA Control and GL12 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)).

The data indicate that in the absence of rapamycin the effect of GL12 knockdown is similar to that induced by rapamycin, albeit weaker (FIG. 15: Grey bars represent all single cells; Vertically shaded bars represent the cell population in the G1 phase of the cell cycle; horizontally shaded bars represent the cells in the G2 phase of the cell cycle. Lighter shades represent cells treated with Culture medium, siRNA Control and GL12 siRNA alone. Darker shades represent cells treated with additional 100 ng/ml rapamycin. All data are normalised to Control (100%)). However, in the presence of rapamycin GL12 knockdown had no further significant effect on p-tau expression in cells.

The data provide evidence that modulation of GL12 has a similar effect to rapamycin in terms of cell cycle and AD-related p-tau expression.

In summary, the modulation of individual rapamycin-sensitive genes can achieve the same beneficial effect on neurones as rapamycin.

Example 3 Modulation of mTOR Activity can be Detected by Imaging Metabolic Markers Associated with Rapamycin-Sensitive Genes

3.1 MRI

To analyse the effect of mTOR activation and inhibition on the brain, SD rats (170-220 g) were treated with rapamycin (inhibitor of mTOR; 0.2 mg/kg i.p.) and ketamine (activator of mTOR; 30 mg/kg i.p) and neuroimaging results from these experiments were compared to control (untreated) animals. There were three animals (n=3) in each group. Animals were sacrificed and the brain removed and frozen for imaging studies.

Whole organs were fixed in 0.154 M LiCl in 10:1 H₂O: formaldehyde prior to MRI experiments. All imaging experiments were performed on a Bruker DMX300 spectrometer, at a ¹H NMR resonance frequency of 300 MHz at 289.5±0.2 K. All images were acquired using a 30 mm radiofrequency resonator. Images were acquired using a spin-echo imaging technique [1]. A set of either 7 or 8 equally spaced, coronal slices of 1 mm thickness, with a matrix size of 128×32 pixels and field-of-view of 30 mm×10 mm, were collected along the length of the brain. The recovery time was 15 s, to ensure full T1 relaxation between each acquisition. A T2 map, for each coronal slice, was produced by acquiring between 16 and 24 echo images and varying the echo time from a minimum value of 3 ms to a maximum value of 80 ms. These echo images were then fitted to Equation 1, resulting in a T2 value for each pixel in the coronal slice.

$\begin{matrix} {M_{x} = {M_{0}e^{\frac{- t}{T_{2}}}}} & (1) \end{matrix}$ where M_(x) is the signal intensity for each pixel at time t and M₀ is the signal intensity at t=0.

A transverse T2 map was acquired for each brain using the method described for the coronal maps. Each image comprised 128×128 pixel array, with a field of view of 3 cm×3 cm. A total of 24 echo images were acquired for each transverse T₂ map, with echo times from 3-80 ms. Each transverse slice was positioned in the centre of the brain.

FIGS. 16A-C show clear differences in the T2 weighted MRI images obtained from Rapamycin treated, ketamine treated and Control animals.

3.2 Magnetic Resonance Spectroscopy Imaging

In silico simulations of the effects of mTOR activation and inhibition on the accumulation of choline and creatine have been carried out. These simulations indicated that mTOR modulation leads to significant changes in choline and creatine levels. This is consistent with the possibility of imaging mTOR activation/inhibition in the brain using magnetic spectroscopy.

Methods

All MSI imaging experiments were performed on a Bruker ultrafleXtreme TOF/TOF mass spectrometer. For matrix evaluation, 4 serial sections of thickness 10 μm from sham control brain S2 were acquired using a Leica CM 1850 Cryostat and subsequently thaw mounted onto an ITO coated glass slide. Each section in turn was coated with 15 mL of 20 mg mL⁻¹ of CHCA in CH₃OH, 0.1% TFA) using an artist airbrush while the remaining 2 sections were covered. Data were collected over the mass range m/z 60-1400. MSI experiments of a single section from each group (Rapa, Ket and Control) were conducted. Data were collected over the mass range m/z 60-1400. Images were acquired with a pixel size of 100 μm×100 μm.

The data set contains numerous ion images which demonstrate grey and white anatomical differences and clear differences induced by mTOR inhibition or activation (by rapamycin and ketamine respectively relative to control). These molecular species belong to the group of Phosphatidylcholines (FIG. 17. First row Rapamycin treated; Second row—Ketamine treated; Third row—Control. Columns: 1) m/z 769, 2) m/z 868, 3) m/z 866, 4) m/z 752, 5) m/z 844, 6) m/z 840, 7) m/z 780).

Additionally there is evidence that, similar to the simulated models, mTOR modulation (by rapamycin or Ketamine) leads to measureable changes of choline (FIG. 18A. First row—Rapamycin treated, Second row—Ketamine treated, Third row—Control) and creatine (FIG. 18B. First row—Rapamycin treated, Second row—Ketamine treated, Third row—Control) levels in the brain.

The clear differences in the MRI imaging as well as the differences in the magnetic spectroscopy indicate that changes in brain metabolism induced by mTOR inhibition or activation can clearly be identified using methods already used in human imaging technology.

Example 4 the Effect of Genetic Polymorphisms on the Rapamycin-Regulated Genes is Associated with the Rapamycin Response in Human Lymphocytes from Individual Patients and the Diagnosis of AD

4.1 in Silico Data Mining

Existing databases were analysed to identify the mTOR regulated genes on the chromosomal regions identified to be linked to AD (linkage studies, AlzGene).

The AlzGene database identifies the following chromosomal regions in linkage with AD (Table 12)

TABLE 12 Location Hamshere et al. (2007) Butler et al. (2009) Chromosome (Mb) LOD (Mb) P-value 1p31.1-q31.1  83-185 0.004-0.05 3q12.3-q25.31 103-173 0.03 6p21.1-q15 43-91 0.02 7pter-q21.11  0-78 0.008-0.04 8p22-p21.1 13-28  0.001 9p22.3-p13.3 20-35 1.2 (~23 Mb) 9q21.31-q32  80-100  2.5 (~101 Mb) 10p14-q24  10-100 3.3 (~61 Mb) 17q24.3-qter 67-79 0.03 19p13.3-qter  8-54 2.0 (~52 Mb)  0.01-0.05

Linkage regions in this table are based on results of the joint and meta-analyses of previously published genome-wide linkage (GWL) data (Hamshere, M. L., P. A. Holmans, et al. (2007). Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Hum Mol Genet 16(22): 2703-12; Butler, A. W., M. Y. Ng, et al. (2009). Meta-analysis of linkage studies for Alzheimer's disease—a web resource. Neurobiol. Aging 30(7): 1037-47).

Genes on the regions identified by AlzGene to be in linkage with AD were identified from the Ensembl database (http://www.ensembl.org). Variations on the genes in the region were identified using BioMart and the Ensembl variation 72 database, the contents of which are incorporated herein in their entirety. The results indicate that 22.17% of rapamycin-regulated genes were found on these AD-related chromosomal regions. Interestingly enough a much smaller number of genes were found to be related to AD in prior studies (see Table 13)

SNPs selected for analysis are shown in Table 14. Further details of each of these SNPs can be found in the NCBI database dbSNP (http://www.ncbi.nlm.nih.gov/SNP/). The contents of the dbSNP database entries for each of the SNPs listed in Table 14 are expressly incorporated herein by reference, in particular for the purposes of further defining the location and identity of the SNP.

TABLE 13 No of % genes % of No of genes rapa- Genes in regulated Rapa associated % genes % of AD No of regulated region % by regulated with AD associated associated genes on genes on of whole Rapa in genes in (from existing with AD in genes in Region region the region genome region this region databases) this region this region 1p31.1-q31.1 1575 46 7.88 2.92 4.38 13 0.83 3.19 3q12.3-q25.31 640 34 3.20 5.31 3.24 5 0.78 1.23 6p21.1-q15 204 10 1.02 4.90 0.95 0 0.00 0.00 7pter-q21.11 991 40 4.96 4.04 3.81 7 0.71 1.72 8p22-p21.1 167 7 0.84 4.19 0.67 5 2.99 1.23 9p22.3-p13.3 275 6 1.38 2.18 0.57 2 0.73 0.49 9q21.31-q32 430 12 2.15 2.79 1.14 5 1.16 1.23 10p14-q24 1072 37 5.36 3.64 3.71 11 1.03 2.70 17q24.3-qter 335 17 1.68 5.07 1.62 1 0.30 0.25 19p13.3-qter 1164 22 5.82 1.89 2.09 11 0.95 2.70 Total 6853 233 34.27 3.40 22.17 60 0.88 14.74

TABLE 14 SNPs selected for analysis 1000 genomes Position on global Associated Distance Variation Chromosome Variant MAF gene with to Code Name Chromosome (bp) Alleles (ALL) phenotype transcript pr1  rs798893  19 54793830 G/C 0.2921 LILRB2, intronic 4072 pr10 rs725106  1 190347665 G/A 0.375 FAM5C intronic 99094 pr11 rs1341665 1 159691559 G/A 0.3814 CRP pr12 rs1359059 1 167234166 G/A 0.4725 POU2F1 intronic* 44038 pr13 rs1532278 8 27466315 T/C 0.2821 CLU 2420 pr14 rs1801274 1 161479745 A/G 0.4304 FCGR2A 395 pr15 rs2036108 8 26663100 C/T 0.2688 ADRA1A intronic** 57433 pr2  rs811925  6 106547372 C/G 0.136 PRDM1, intronic**** 212 pr3  rs883524  8 23194591 T/C 0.1401 LOXL2 intronic*** 3583 pr4  rs1065457 1 158324425 A/G 0.4469 CD1E intronic 646 pr5  rs1148613 1 190337300 A/C 0.3723 FAM5C intronic 106583 pr6  rs295     8 19816238 A/C 0.2596 LPL 4576 pr7  rs290258  9 93555739 A/G 0.2592 SYK pr8  rs365836  7 101809851 A/G 0.2601 CUX1 117399 pr9  rs569214  8 27487790 G/T 0.3539 CLU 3595

The SNPs selected were either SNPs on mTOR-sensitive genes or their direct upstream regulators (POU2F1 is a transcriptional regulator of the mTOR genes A2M, CRP, CSF1R, CYP2C9, ESR1, GSTM3, IL2, IL6, PRKAA2, SPP1, TLR4 from Table 1; ADRA1A is a regulator of mTOR regulated genes: CDKN1B, EGR1, FGF7, FN1, IL6, JUN, LOX, NR4A1, NR4A2 from Table 1; LOXL2 is an upstream regulator of mTOR regulated genes: CDH1, FN1, MMP9 from Table 1; PRDM1 is the upstream regulator of mTOR regulated genes: ESR1, IGHG1, IL10, IL2, IL6, MYC, RELN, SCGN from Table 1).

Methods

The rapamycin response in peripheral lymphocytes was measured in 39 patients. The method has been described previously (Yates et al, Dysfunction of the mTOR pathway is a risk factor for Alzheimer's disease, Acta Neuropathological Communications, 2013).

Genomic DNA was extracted from the same lymphocyte samples (using established protocols). Primers were designed for the SNPs in Table 13 using Primer3 tool. PCR was carried out using the 2×Reddymix PCR master mix (Thermo scientific, AB-0575/DC/LD/B) with a final composition of: 0.625 units ThermoPrime Taq DNA polymerase, 75 mM Tris-HCl (pH 8.8 at 25° C.), 20 mM (NH₄)₂SO₄, 1.5 Mm MgCl₂, 0.01% (v/v) Tween 20, 0.2 mM each of dATP, dCTP, dGTP and dTTP, and precipitant and red dye for electrophoresis.

PCR Mix was Assembled as Follows:

P21 ex2 (Forward Primer) 0.2 μl P21 ex2′ (Reverse Primer) 0.2 μl Nuclease free water 15.6 μl  2 x Reddy Mix PCR master mix  20 μl

The reagents were added in the volumes as stated above to give a 36 μl Master Mix′. The Master Mix is dispensed in 36 μl aliquots, to which is added 4 μl of test DNA. The PCR was carried out as follows: 95° C. for 5 minutes, followed by 40 cycles of 95° C. for 60 sec, 57° C. for 60 sec and 72° C. for 60 sec.

Following the PCR 4 μl of each sample was denatured in 12 μl SSCP denaturing solution (95% Formamide, 10 mM NaOH, 0.01% w/v xylene cyanole and 0.01% w/v bromophenol blue). Samples were denatured at 95° C. for 6 minutes and placed on ice for at least 10 minutes. Gel electrophoresis was performed using 3% Metaphore agarose+0.5% multipurpose agarose gels, at 400 V for 45 minutes.

The SNPs on the samples lead to single stranded variants that ran at different speeds on the gel (SSCP analysis).

The variant with the lower frequency was regarded the minor allele and labelled “1”; while the more frequent allele was labelled “0”.

4.2 Minor Allele Frequencies and the Association of these Alleles with AD.

As the Chi-squared analyses indicated, none of the SNPs investigated was significantly associated on their own with the diagnosis of AD (see Tables 15-29).

TABLE 15 Frequency table & Chi-squared test Codes X pr1 Codes Y DG Codes X Codes Y 0 1 CONTROL 13 7 20 (51.3%) PROB. AD 14 5 19 (48.7%) 27 12 39 (69.2%) (30.8%) Chi-squared 0.058 DF 1 Significance level P = 0.8101 Contingency coefficient 0.038

TABLE 16 Frequency table & Chi-squared test Codes X pr10 Codes Y DG Codes X Codes Y 0 1 CONTROL 17 3 20 (51.3%) PROB. AD 13 6 19 (48.7%) 30 9 39 (76.9%) (23.1%) Chi-squared 0.719 DF 1 Significance level P = 0.3964 Contingency coefficient 0.135

TABLE 17 Frequency table & Chi-squared test Codes X pr11 Codes Y DG Codes X Codes Y 0 1 CONTROL 14 6 20 (51.3%) PROB. AD 13 6 19 (48.7%) 27 12 39 (69.2%) (30.8%) Chi-squared 0.058 DF 1 Significance level P = 0.8101 Contingency coefficient 0.038

TABLE 18 Frequency table & Chi-squared test Codes X pr12 Codes Y DG Codes X Codes Y 0 1 CONTROL 15 5 20 (51.3%) PROB. AD 13 6 19 (48.7%) 28 11 39 (71.8%) (28.2%) Chi-squared 0.010 DF 1 Significance level P = 0.9200 Contingency coefficient 0.016

TABLE 19 Frequency table & Chi-squared test Codes X pr13 Codes Y DG Codes X Codes Y 0 1 CONTROL 13 7 20 (51.3%) PROB. AD 11 8 19 (48.7%) 24 15 39 (61.5%) (38.5%) Chi-squared 0.016 DF 1 Significance level P = 0.8992 Contingency coefficient 0.020

TABLE 20 Frequency table & Chi-squared test Codes X pr14 Codes Y DG Codes X Codes Y 0 1 CONTROL 15 5 20 (51.3%) PROB. AD 15 4 19 (48.7%) 30 9 39 (76.9%) (23.1%) Chi-squared 0.008 DF 1 Significance level P = 0.9301 Contingency coefficient 0.014

TABLE 21 Frequency table & Chi-squared test Codes X pr15 Codes Y DG Codes X Codes Y 0 1 CONTROL 12 8 20 (51.3%) PROB. AD 12 7 19 (48.7%) 24 15 39 (61.5%) (38.5%) Chi-squared 0.016 DF 1 Significance level P = 0.8992 Contingency coefficient 0.020

TABLE 22 Frequency table & Chi-squared test Codes X pr2 Codes Y DG Codes X Codes Y 0 1 CONTROL 16 4 20 (51.3%) PROB. AD 17 2 19 (48.7%) 33 6 39 (84.6%) (15.4%) Chi-squared 0.141 DF 1 Significance level P = 0.7072 Contingency coefficient 0.060

TABLE 23 Frequency table & Chi-squared test Codes X pr3 Codes Y DG Codes X Codes Y 0 1 CONTROL 10 10 20 (51.3%) PROB. AD 10 9 19 (48.7%) 20 19 39 (51.3%) (48.7%) Chi-squared 0.024 DF 1 Significance level P = 0.8759 Contingency coefficient 0.025

TABLE 24 Frequency table & Chi-squared test Codes X pr4 Codes Y DG Codes X Codes Y 0 1 CONTROL 20 0 20 (51.3%) PROB. AD 15 4 19 (48.7%) 35 4 39 (89.7%) (10.3%) Chi-squared 2.683 DF 1 Significance level P = 0.1014 Contingency coefficient 0.254

TABLE 25 Frequency table & Chi-squared test Codes X pr5 Codes Y DG Codes X Codes Y 0 1 CONTROL 16 4 20 (51.3%) PROB. AD 14 5 19 (48.7%) 30 9 39 (76.9%) (23.1%) Chi-squared 0.008 DF 1 Significance level P = 0.9301 Contingency coefficient 0.014

TABLE 26 Frequency table & Chi-squared test Codes X pr6 Codes Y DG Codes X Codes Y 0 1 CONTROL 9 11 20 (51.3%) PROB. AD 11 8 19 (48.7%) 20 19 39 (51.3%) (48.7%) Chi-squared 0.235 DF 1 Significance level P = 0.6278 Contingency coefficient 0.077

TABLE 27 Frequency table & Chi-squared test Codes X pr7 Codes Y DG Codes X Codes Y 0 1 CONTROL 17 3 20 (51.3%) PROB. AD 14 5 19 (48.7%) 31 8 39 (79.5%) (20.5%) Chi-squared 0.229 DF 1 Significance level P = 0.6326 Contingency coefficient 0.076

TABLE 28 Frequency table & Chi-squared test Codes X pr8 Codes Y DG Codes X Codes Y 0 1 CONTROL 14 6 20 (51.3%) PROB. AD 15 4 19 (48.7%) 29 10  39 (74.4%) (25.6%) Chi-squared 0.074 DF 1 Significance level P = 0.7850 Contingency coefficient 0.044

TABLE 29 Frequency table & Chi-squared test Codes X pr9 Codes Y DG Codes X Codes Y 0 1 CONTROL 16 4 20 (51.3%) PROB. AD 16 3 19 (48.7%) 32 7 39 (82.1%) (17.9%) Chi-squared 0.006 DF 1 Significance level P = 0.9403 Contingency coefficient 0.012

However, when combinations of SNPs were investigated, it was found that different combinations of SNPs were significantly associated with the rapamycin response of the individual patient as measured from lymphocytes.

The increase in cell death elicited by rapamycin in the lymphocytes was significantly associated with the combination of pr4, pr1 and pr15 (Table 30).

TABLE 30 Multiple regression Dependent Y f_DEAD_Rapa/f_DEAD_Control Sample size 39 Coefficient of determination R² 0.2305 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.0999 pr4 0.7790 0.4291 0.2933 1.815 0.0781 pr1 −0.7175 0.3987 −0.2910 −1.800 0.0805 pr15 0.8547 0.3871 0.3497 2.208 0.0339 F-ratio 3.4942 Significance level P = 0.026

The relative lengthening of the G1 time induced by rapamycin in the lymphocyte cultures (as defined in Zs Nagy, M Combrinck, M Budge, R McShane. Cell cycle kinesis in lymphocytes in the diagnosis of Alzheimer's disease. Neurosci Letters. 2002, 317, 2, 81-84) was significantly associated with a combination of pr4, pr5, pr7, pr10 and pr11 (Table 31).

TABLE 31 Multiple regression Dependent Y Relative lengthening of G1 time Sample size 39 Coefficient of determination R² 0.4594 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 0.9648 pr4 0.3609 0.1148 0.4802 3.145 0.0035 pr5 −0.3738 0.1476 −0.4033 −2.532 0.0163 pr7 0.2966 0.1120 0.4187 2.649 0.0123 pr10 0.2171 0.08211 0.4182 2.644 0.0124 pr11 0.3363 0.1350 0.3979 2.492 0.0179 F-ratio 5.6095 Significance level P = 0.001

The difference between population doubling level induced by Rapamycin in the lymphocyte cultures was significantly associated with the combination of pr4, pr6, pr12, pr13, pr1, pr8, pr10 and pr11 (Table 32).

TABLE 32 Multiple regression Dependent Y difference between population doubling level induced by Rapamycin Sample size 39 Coefficient of determination R² 0.5932 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 0.7941 pr4 −0.3640 0.1715 −0.3614 −2.123 0.0421 pr6 −0.2529 0.1572 −0.2818 −1.609 0.1182 pr12 −0.6737 0.1633 −0.6016 −4.125 0.0003 pr13 −0.2117 0.1259 −0.2936 −1.682 0.1029 pr1 −0.2015 0.1414 −0.2517 −1.424 0.1646 pr8 0.3235 0.1766 0.3172 1.832 0.0769 pr10 0.4391 0.1160 0.5684 3.784 0.0007 pr11 −0.2514 0.1759 −0.2524 −1.429 0.1633 F-ratio 5.4687 Significance level P < 0.001

This association was significantly affected by the plasma homocysteine levels of the patients measured at the time of the blood sample collection. Plasma homocysteine is an independent environmental risk factor of AD and it is also known to affect cell proliferation and cell cycle control functions (Table 33).

TABLE 33 Multiple regression Dependent Y difference between population doubling level induced by Rapamycin Sample size 39 Coefficient of determination R² 0.5954 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.1601 pr12 −0.5319 0.1663 −0.4982 −3.199 0.0032 pr3 −0.4043 0.1423 −0.4544 −2.840 0.0079 pr8 0.3558 0.1715 0.3492 2.075 0.0464 pr10 0.4772 0.1190 0.5844 4.010 0.0004 pr11 −0.3726 0.1756 −0.3562 −2.122 0.0419 pr15 −0.2380 0.1250 −0.3235 −1.904 0.0663 LHcy −0.03578 0.01574 −0.3779 −2.272 0.0301 F-ratio 6.5158 Significance level P < 0.001

The change in the G1 time induced by Rapamycin in lymphocyte cultures was significantly associated with pr5, pr7, pr10, pr11 and pr15 (Table 34).

TABLE 34 Multiple regression Dependent Y avg_TG1′/avg_TG1 Sample size 39 Coefficient of determination R² 0.4968 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.2308 pr5 −0.8739 0.1888 −0.6274 −4.628 0.0001 pr7 0.2405 0.1438 0.2796 1.673 0.1038 pr10 0.3729 0.1063 0.5212 3.508 0.0013 pr11 0.5171 0.1789 0.4495 2.891 0.0068 pr15 −0.2051 0.1068 −0.3171 −1.921 0.0634 F-ratio 6.5156 Significance level P < 0.001

The significant association between the SNPs on rapamycin-sensitive genes and the change in the G1 time induced by rapamycin in lymphocyte cultures was altered by plasma homocysteine levels (Table 35).

TABLE 35 Dependent Y avg_TG1′/avg_TG1 Sample size 39 Coefficient of determination R² 0.5859 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.6011 pr5 −0.7138 0.1943 −0.5569 −3.673 0.0009 pr7 0.2224 0.1432 0.2727 1.552 0.1311 pr13 0.2103 0.1296 0.2840 1.623 0.1151 pr3 −0.2627 0.1554 −0.2949 −1.691 0.1013 pr10 0.3731 0.1071 0.5365 3.482 0.0015 pr11 0.3414 0.1894 0.3126 1.803 0.0815 pr15 −0.1511 0.1129 −0.2374 −1.338 0.1908 LHcy −0.02881 0.01399 −0.3519 −2.059 0.0483 F-ratio 5.3058 Significance level P < 0.001

The baseline proliferation speed (population doubling time PDT) of the lymphocytes from individual patients also depended on a combination of SNPs (pr4, pr5, pr6, pr12, pr13, pr14, pr1, pr11 and pr15) (Table 36).

TABLE 36 Multiple regression Dependent Y avg_PDT avg PDT Sample size 39 Coefficient of determination R² 0.6676 Regression Equation Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 9.0610 pr4 12.3884 3.2678 0.5756 3.791 0.0007 pr5 −18.7518 6.3679 −0.4798 −2.945 0.0063 pr6 6.3645 3.1861 0.3478 1.998 0.0552 pr12 14.3572 4.6488 0.4975 3.088 0.0044 pr13 4.1192 2.3607 0.3082 1.745 0.0916 pr14 −9.8338 4.4575 −0.3791 −2.206 0.0354 pr1 −4.5430 3.0234 −0.2688 −1.503 0.1438 pr11 22.4197 4.2262 0.7018 5.305 <0.0001 pr15 5.8245 3.0380 0.3354 1.917 0.0651 F-ratio 6.4729 Significance level P < 0.001

This relationship was also significantly affected by plasma homocysteine levels (Table 37).

TABLE 37 Multiple regression Dependent Y avg_PDT avg PDT Sample size 39 Coefficient of determination R² 0.6897 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 4.1698 pr4 10.4761 3.4882 0.4936 3.003 0.0056 pr5 −18.3444 6.2689 −0.4839 −2.926 0.0067 pr6 7.1093 3.1775 0.3894 2.237 0.0334 pr12 12.5726 4.7438 0.4478 2.650 0.0131 pr13 4.3352 2.3266 0.3321 1.863 0.0729 pr14 −9.7313 4.3841 −0.3868 −2.220 0.0347 pr1 −6.0997 3.1717 −0.3416 −1.923 0.0647 pr11 22.9197 4.1712 0.7203 5.495 <0.0001 pr15 5.8184 2.9876 0.3454 1.947 0.0616 LHcy 0.4774 0.3386 0.2574 1.410 0.1697 F-ratio 6.2226 Significance level P < 0.001

The change induced in cell proliferation (PDT) by rapamycin was also significantly associated with a combination of SNPs on rapamycin-sensitive genes (pr4, pr5, pr7, pr10, pr11, pr15) (Table 38) and the association was significantly affected by plasma homocysteine levels (Table 39).

TABLE 38 Multiple regression Dependent Y avg_PDT′_PDT avg PDT′/PDT Sample size 39 Coefficient of determination R² 0.4664 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.2206 pr4 −0.1752 0.1156 −0.2587 −1.515 0.1396 pr5 −0.6109 0.1468 −0.5927 −4.162 0.0002 pr7 0.1782 0.1118 0.2713 1.594 0.1207 pr10 0.2466 0.08267 0.4664 2.983 0.0054 pr11 0.3134 0.1393 0.3695 2.249 0.0315 pr15 −0.1211 0.08413 −0.2465 −1.439 0.1598 F-ratio 4.6613 Significance level P = 0.002

TABLE 39 Multiple regression Dependent Y avg_PDT′_PDT avg PDT′/PDT Sample size 39 Coefficient of determination R² 0.5013 R²-adjusted 0.4078 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 1.5047 pr5 −0.5644 0.1456 −0.5653 −3.877 0.0005 pr7 0.2353 0.1084 0.3583 2.171 0.0375 pr3 −0.1677 0.09174 −0.3074 −1.827 0.0770 pr10 0.2618 0.08455 0.4801 3.096 0.0041 pr11 0.2222 0.1458 0.2602 1.525 0.1372 LHcy −0.02361 0.01068 −0.3638 −2.209 0.0344 F-ratio 5.3610 Significance level P = 0.001

The baseline length of the G1 time in the lymphocyte cultures was significantly associated with a combination of SNPs on the rapamycin-sensitive genes (pr4, pr5, pr6, pr12, pr14, pr1, pr10, pr11 and pr15) (Table 40).

TABLE 40 Multiple Regression Dependent Y avg_TG1 avg TG1 Sample size 39 Coefficient of determination R² 0.6827 Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 7.2421 pr4 9.7224 2.0230 0.6658 4.806 <0.0001 pr5 −8.9847 4.3131 −0.3608 −2.083 0.0462 pr6 3.8481 2.1043 0.3215 1.829 0.0778 pr12 10.2202 3.0217 0.5319 3.382 0.0021 pr14 −8.8697 3.0202 −0.4788 −2.937 0.0064 pr1 −4.4125 1.9865 −0.3813 −2.221 0.0343 pr10 −2.0526 1.4835 −0.2488 −1.384 0.1770 pr11 12.5716 2.7938 0.6412 4.500 0.0001 pr15 6.6133 1.9953 0.5242 3.314 0.0025 F-ratio 6.9327 Significance level P < 0.001

The ‘efficacy of Rapamycin’ in the lymphocyte cultures was also calculated from the combined effect on cell proliferation time and relative lengthening of the G1 time. This estimate was based on idealised cell culture models. The resulting value was significantly associated with a combination of pr4, pr12, pr10 and pr15 (Table 41).

TABLE 41 Multiple regression Dependent Y efficiency_of_Rapa_from_ideal_model efficiency of Rapa from ideal model Sample size 39 Coefficient of 0.3972 determination R² Regression Equation Independent variables Coefficient Std. Error r_(partial) t P (Constant) 0.6211 pr4 −0.5339 0.2317 −0.3676 −2.305 0.0274 pr12 −0.4911 0.1739 −0.4359 −2.824 0.0079 pr10 0.4397 0.1636 0.4186 2.687 0.0111 pr15 −0.4562 0.1653 −0.4279 −2.761 0.0092 F-ratio 5.6012 Significance level P = 0.001 4.3 the Association of the Variants on Rapamycin-Sensitive Genes with AD.

Logistic regression indicates that a combination of pr1, pr10 and plasma homocysteine levels are significantly associated with the diagnosis of AD. The prediction from the model would allow the correct classification of 77.4% of the patients (AUC) (Table 42).

TABLE 42 42.1 Logistic regression Dependent Y DG_AD Select LHcy > 0 Sample size 39 Cases with Y = Control 20 (51.28%) Cases with Y = AD  19 48.72%) 42.2 OVERALL MODEL FIT Null model −2 Log Likelihood 54.040 Significance level P = 0.0162 42.3 COEFFICIENTS AND STANDARD ERRORS Variable Coefficient Std. Error P pr1 = 1 −1.35043 0.90923 0.1375 pr10 = 1 1.69245 0.97968 0.0841 LHcy 0.35371 0.14382 0.0139 Constant −3.9978 42.4 ODDS RATIOS AND 95% CONFIDENCE INTERVALS Variable Odds ratio 95% CI pr1 = 1 0.2591 0.0436 to 1.5398 pr10 = 1 5.4328  0.7963 to 37.0631 LHcy 1.4243 1.0745 to 1.8881 42.5 CLASSIFICATION TABLE (CUT-OFF VALUE P = 0.5) Predicted group Actual group 0 1 Percent correct Y = Control 15 5 75.00% Y = AD 7 12 63.16% Percent of cases 69.23% correctly classified 42.6 ROC CURVE ANALYSIS Area under the ROC curve (AUC) 0.774 Standard Error 0.0769 95% Confidence interval 0.612 to 0.892

In summary the data presented indicate that the rapamycin response in peripheral lymphocytes from individual patients is the result of the combination of SNPs on the rapamycin-sensitive genes. The data also show that this genetic association is strongly dependent on an environmental risk factor that has an influence on cell proliferation and cell cycle characteristics, and is itself an independent risk factor for AD.

The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying figures. Such modifications are intended to fall within the scope of the appended claims. Moreover, all aspects and embodiments of the invention described herein are considered to be broadly applicable and combinable with any and all other consistent embodiments, including those taken from other aspects of the invention (including in isolation) as appropriate.

Various publications are cited herein, the disclosures of which are incorporated by reference in their entireties. 

The invention claimed is:
 1. A method for detection of a combination of human single nucleotide polymorphisms (SNPs) in a human subject, comprising a) obtaining a nucleic acid sample from said human subject; b) genotyping the sample for a combination of SNPs in rapamycin-sensitive gene(s) CD1E, LPL, POU2F1, CLU, LILRB2, CUX1, FAM5C, and CRP, said combination of SNP alleles being rs1065457 (G), rs295 (C), rs1359059 (A), rs1532278 (C), rs798893 (C), rs365836 (G), rs725106 (A), rs1341665 (A); and c) detecting in said nucleic acid sample from said human subject the presence of a G for rs1065457, a C for rs295, an A for rs1359059, a C for rs1532278, a C for rs798893, a G for rs365836, an A for rs725106, and an A for rs1341665.
 2. The method of claim 1, further comprising detection of one or more SNP alleles selected from rs1148613 (C), rs290258 (G), rs2036108 (T), rs1801274 (G), rs811925 (G), rs883524 (C), and rs569214 (T).
 3. The method of claim 2, where all SNP alleles are detected. 